431 88 0 http://purl.obolibrary.org/obo/MONDO_0800028 dyskinesia with orofacial involvement, autosomal dominant 'dyskinesia with orofacial involvement, autosomal dominant' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0800026 central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease 'central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0009005 premature menopause 'premature menopause' SubClassOf 'ovarian dysfunction' http://www.ebi.ac.uk/efo/EFO_0009002 splenic disease 'splenic disease' SubClassOf 'digestive system disease' http://purl.obolibrary.org/obo/UBERON_0002106 spleen 'spleen' SubClassOf 'part of' some 'digestive system' http://www.ebi.ac.uk/efo/EFO_1000146 Breast Mucosa-Associated Lymphoid Tissue Lymphoma 'Breast Mucosa-Associated Lymphoid Tissue Lymphoma' SubClassOf 'integumentary system cancer' 'Breast Mucosa-Associated Lymphoid Tissue Lymphoma' SubClassOf 'integumentary system disease' http://www.ebi.ac.uk/efo/EFO_1000157 Central Nervous System Lymphoma 'Central Nervous System Lymphoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1000174 Chondroid Chordoma 'Chondroid Chordoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011835 sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 'sensory ataxic neuropathy, dysarthria, and ophthalmoparesis' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0011841 biotin-responsive basal ganglia disease 'biotin-responsive basal ganglia disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011876 juvenile absence epilepsy 'juvenile absence epilepsy' SubClassOf 'inherited disease susceptibility' 'juvenile absence epilepsy' SubClassOf 'monogenic epilepsy' 'juvenile absence epilepsy' SubClassOf 'predisposes towards' some 'juvenile absence epilepsy' 'juvenile absence epilepsy' SubClassOf 'adolescent/adult-onset epilepsy syndrome' 'juvenile absence epilepsy' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_1000077 AIDS-Related Primary Central Nervous System Lymphoma 'AIDS-Related Primary Central Nervous System Lymphoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0021272 inherited orthostatic hypotension 'inherited orthostatic hypotension' SubClassOf 'genetic disorder' 'inherited orthostatic hypotension' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0009201 myopic macular degeneration 'myopic macular degeneration' SubClassOf 'genetic disorder' 'myopic macular degeneration' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011738 bilateral frontoparietal polymicrogyria 'bilateral frontoparietal polymicrogyria' SubClassOf 'genetic disorder' 'bilateral frontoparietal polymicrogyria' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011772 B4GALT1-congenital disorder of glycosylation 'B4GALT1-congenital disorder of glycosylation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0021107 narcolepsy 'narcolepsy' SubClassOf 'genetic disorder' 'narcolepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011789 familial meningioma 'familial meningioma' SubClassOf 'genetic disorder' 'familial meningioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0060707 Ververi-Brady syndrome 'Ververi-Brady syndrome' SubClassOf 'genetic disorder' 'Ververi-Brady syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0060760 intellectual developmental disorder with dysmorphic facies and behavioral abnormalities 'intellectual developmental disorder with dysmorphic facies and behavioral abnormalities' SubClassOf 'genetic disorder' 'intellectual developmental disorder with dysmorphic facies and behavioral abnormalities' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0060763 intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities 'intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0009168 response to prednisolone 'response to prednisolone' SubClassOf 'response to glucocorticoid' 'response to prednisolone' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0800468 SCN4A-related channelopathy 'SCN4A-related channelopathy' SubClassOf 'genetic disorder' 'SCN4A-related channelopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0011612 glycine encephalopathy 'glycine encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0009072 mbd5 associated neurodevelopmental disorder 'mbd5 associated neurodevelopmental disorder' SubClassOf 'genetic disorder' 'mbd5 associated neurodevelopmental disorder' SubClassOf 'nervous system disease' 'mbd5 associated neurodevelopmental disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0021022 hereditary hyperekplexia 'hereditary hyperekplexia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0060663 congenital heart defects, multiple types, 5 'congenital heart defects, multiple types, 5' SubClassOf 'genetic disorder' 'congenital heart defects, multiple types, 5' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 'congenital heart defects, multiple types, 5' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100541 http://purl.obolibrary.org/obo/MONDO_0045018 creatine biosynthetic process disease 'creatine biosynthetic process disease' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0045020 glycine metabolism disease 'glycine metabolism disease' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0800183 PAX6-related ocular dysgenesis 'PAX6-related ocular dysgenesis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011506 familial infantile myoclonic epilepsy 'familial infantile myoclonic epilepsy' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0011514 tricuspid atresia 'tricuspid atresia' SubClassOf 'genetic disorder' 'tricuspid atresia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0011510 Bohring-Opitz syndrome 'Bohring-Opitz syndrome' SubClassOf 'genetic disorder' 'Bohring-Opitz syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011551 TH-deficient dopa-responsive dystonia 'TH-deficient dopa-responsive dystonia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.orpha.net/ORDO/Orphanet_371439 Genetic cerebrovascular dementia 'Genetic cerebrovascular dementia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011400 dilated cardiomyopathy 1G 'dilated cardiomyopathy 1G' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011454 patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome 'patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome' SubClassOf 'heart disease' 'patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0016143 qualitative or quantitative defects of gamma-sarcoglycan 'qualitative or quantitative defects of gamma-sarcoglycan' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of gamma-sarcoglycan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016144 qualitative or quantitative defects of delta-sarcoglycan 'qualitative or quantitative defects of delta-sarcoglycan' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of delta-sarcoglycan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016145 qualitative or quantitative defects of dysferlin 'qualitative or quantitative defects of dysferlin' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of dysferlin' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016146 caveolinopathy 'caveolinopathy' SubClassOf 'genetic disorder' 'caveolinopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016141 qualitative or quantitative defects of alpha-sarcoglycan 'qualitative or quantitative defects of alpha-sarcoglycan' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of alpha-sarcoglycan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016142 qualitative or quantitative defects of beta-sarcoglycan 'qualitative or quantitative defects of beta-sarcoglycan' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of beta-sarcoglycan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016155 qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 'qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016151 qualitative or quantitative defects of perlecan 'qualitative or quantitative defects of perlecan' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of perlecan' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016153 qualitative or quantitative defects of TRIM32 'qualitative or quantitative defects of TRIM32' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of TRIM32' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0004829 response to irinotecan 'response to irinotecan' SubClassOf 'response to antineoplastic agent' 'response to irinotecan' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0016192 qualitative or quantitative defects of telethonin 'qualitative or quantitative defects of telethonin' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of telethonin' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016187 qualitative or quantitative defects of desmin 'qualitative or quantitative defects of desmin' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of desmin' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016198 qualitative or quantitative defects of plectin 'qualitative or quantitative defects of plectin' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of plectin' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016195 qualitative or quantitative defects of beta-myosin heavy chain (MYH7) 'qualitative or quantitative defects of beta-myosin heavy chain (MYH7)' SubClassOf 'genetic disorder' 'qualitative or quantitative defects of beta-myosin heavy chain (MYH7)' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016001 2-hydroxyglutaric aciduria '2-hydroxyglutaric aciduria' SubClassOf 'nervous system disease' '2-hydroxyglutaric aciduria' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016027 benign neonatal seizures 'benign neonatal seizures' SubClassOf 'monogenic epilepsy' 'benign neonatal seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016022 early myoclonic encephalopathy 'early myoclonic encephalopathy' SubClassOf 'monogenic epilepsy' 'early myoclonic encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016025 myoclonic-astatic epilepsy 'myoclonic-astatic epilepsy' SubClassOf 'monogenic epilepsy' 'myoclonic-astatic epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0004624 prostate specific antigen measurement 'prostate specific antigen measurement' SubClassOf 'protein measurement' 'prostate specific antigen measurement' SubClassOf 'is_about' some 'prostate gland' 'prostate specific antigen measurement' SubClassOf 'cancer biomarker measurement' 'prostate specific antigen measurement' SubClassOf 'is_about' some ('prostate carcinoma' and ('has_role' some 'biomarker')) 'prostate specific antigen measurement' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0004647 response to platinum based chemotherapy 'response to platinum based chemotherapy' SubClassOf 'response to antineoplastic agent' 'response to platinum based chemotherapy' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/GO_0097328 response to carboplatin 'response to carboplatin' SubClassOf 'response to platinum based chemotherapy' 'response to carboplatin' SubClassOf http://purl.obolibrary.org/obo/OBA_2040037 http://www.ebi.ac.uk/efo/EFO_1000805 angioid streaks 'angioid streaks' SubClassOf 'genetic disorder' 'angioid streaks' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1000825 atrial heart septal defect 'atrial heart septal defect' SubClassOf 'genetic disorder' 'atrial heart septal defect' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_1000940 Frey Syndrome 'Frey Syndrome' SubClassOf 'genetic disorder' 'Frey Syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0004895 Tourette syndrome 'Tourette syndrome' SubClassOf 'genetic disorder' 'Tourette syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1000630 marginal zone B-cell lymphoma 'marginal zone B-cell lymphoma' SubClassOf 'gastrointestinal lymphoma' http://www.ebi.ac.uk/efo/EFO_1000645 orthostatic intolerance 'orthostatic intolerance' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/HP_0000649 Abnormality of visual evoked potentials 'Abnormality of visual evoked potentials' SubClassOf 'Abnormal nervous system physiology' http://www.ebi.ac.uk/efo/EFO_1000453 Paraganglioma 'Paraganglioma' SubClassOf 'genetic disorder' 'Paraganglioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0700126 alpha-crystallinopathy 'alpha-crystallinopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1000543 Spinal Chordoma 'Spinal Chordoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0031037 famililal cerebral cavernous malformations 'famililal cerebral cavernous malformations' SubClassOf 'genetic disorder' 'famililal cerebral cavernous malformations' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005269 congenital heart malformation 'congenital heart malformation' SubClassOf 'genetic disorder' 'congenital heart malformation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0002404 liver hemangioma 'liver hemangioma' SubClassOf 'benign digestive system neoplasm' 'liver hemangioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0859689 http://www.ebi.ac.uk/efo/EFO_0005205 response to dabigatran etexilate 'response to dabigatran etexilate' SubClassOf 'response to anticoagulant' 'response to dabigatran etexilate' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0005202 response to hydrochlorothiazide 'response to hydrochlorothiazide' SubClassOf 'response to thiazide' 'response to hydrochlorothiazide' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/HP_0000735 Impaired social interactions 'Impaired social interactions' SubClassOf 'Atypical behavior' 'Impaired social interactions' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0005422 skin aging 'skin aging' SubClassOf 'developmental process' 'skin aging' SubClassOf http://www.ebi.ac.uk/efo/EFO_0022597 http://purl.obolibrary.org/obo/MONDO_0016820 Moyamoya disease 'Moyamoya disease' SubClassOf 'genetic disorder' 'Moyamoya disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0002070 ventricular septal defect 'ventricular septal defect' SubClassOf 'genetic disorder' 'ventricular septal defect' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0100523 SPAST-related motor disorder 'SPAST-related motor disorder' SubClassOf 'genetic disorder' 'SPAST-related motor disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005304 atrial conduction disease 'atrial conduction disease' SubClassOf 'genetic disorder' 'atrial conduction disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0100500 Mendelian neurodevelopmental disorder 'Mendelian neurodevelopmental disorder' SubClassOf 'genetic disorder' 'Mendelian neurodevelopmental disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016525 familial hyperaldosteronism 'familial hyperaldosteronism' SubClassOf 'hyperaldosteronism' http://purl.obolibrary.org/obo/MONDO_0016543 hyperphenylalaninemia due to tetrahydrobiopterin deficiency 'hyperphenylalaninemia due to tetrahydrobiopterin deficiency' SubClassOf 'inborn disorder of amino acid and other organic acid metabolism' 'hyperphenylalaninemia due to tetrahydrobiopterin deficiency' SubClassOf 'inborn errors of metabolism' http://purl.obolibrary.org/obo/MONDO_0016558 familial congenital mirror movements 'familial congenital mirror movements' SubClassOf 'genetic disorder' 'familial congenital mirror movements' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005655 response to cytosine arabinoside 'response to cytosine arabinoside' SubClassOf 'response to antineoplastic agent' 'response to cytosine arabinoside' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/UBERON_2000677 segmental intercostal artery 'segmental intercostal artery' SubClassOf 'part of' some 'thoracic aorta' http://purl.obolibrary.org/obo/MONDO_0016483 intracranial berry aneurysm 'intracranial berry aneurysm' SubClassOf 'genetic disorder' 'intracranial berry aneurysm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100284 X-linked intellectual disability 'X-linked intellectual disability' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005526 response to alcohol 'response to alcohol' SubClassOf 'response to stimulus' 'response to alcohol' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0005581 red-green color blindness 'red-green color blindness' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005580 red color blindness 'red color blindness' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100196 TPM2-related myopathy 'TPM2-related myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100172 intellectual disability, autosomal dominant 'intellectual disability, autosomal dominant' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100175 TTN-related myopathy 'TTN-related myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016349 congenital hydrocephalus 'congenital hydrocephalus' SubClassOf 'genetic disorder' 'congenital hydrocephalus' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100154 TUBB3-related tubulinopathy 'TUBB3-related tubulinopathy' SubClassOf 'genetic disorder' 'TUBB3-related tubulinopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100147 SATB2 associated disorder 'SATB2 associated disorder' SubClassOf 'genetic disorder' 'SATB2 associated disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005917 generalised epilepsy 'generalised epilepsy' SubClassOf 'monogenic epilepsy' 'generalised epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 'generalised epilepsy' SubClassOf 'epilepsy' http://www.ebi.ac.uk/efo/EFO_0005853 response to silica exposure 'response to silica exposure' SubClassOf 'response to stimulus' 'response to silica exposure' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0100084 alpha-actinopathy 'alpha-actinopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0016215 spastic quadriplegic cerebral palsy 'spastic quadriplegic cerebral palsy' SubClassOf 'genetic disorder' 'spastic quadriplegic cerebral palsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100009 structural congenital heart disease, multiple types - GATA4 'structural congenital heart disease, multiple types - GATA4' SubClassOf 'genetic disorder' 'structural congenital heart disease, multiple types - GATA4' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0016296 holoprosencephaly 'holoprosencephaly' SubClassOf 'genetic disorder' 'holoprosencephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0100108 TPM3-related myopathy 'TPM3-related myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0005773 retinal detachment 'retinal detachment' SubClassOf 'genetic disorder' 'retinal detachment' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012611 polyhydramnios, megalencephaly, and symptomatic epilepsy 'polyhydramnios, megalencephaly, and symptomatic epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012637 COG1-congenital disorder of glycosylation 'COG1-congenital disorder of glycosylation' SubClassOf 'heart disease' 'COG1-congenital disorder of glycosylation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0036696 spleen neoplasm 'spleen neoplasm' SubClassOf 'digestive system neoplasm' http://purl.obolibrary.org/obo/MONDO_0012586 coronary artery disease, autosomal dominant 2 'coronary artery disease, autosomal dominant 2' SubClassOf 'genetic disorder' 'coronary artery disease, autosomal dominant 2' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0012593 brain-lung-thyroid syndrome 'brain-lung-thyroid syndrome' SubClassOf 'genetic disorder' 'brain-lung-thyroid syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012391 neuronal ceroid lipofuscinosis 8 northern epilepsy variant 'neuronal ceroid lipofuscinosis 8 northern epilepsy variant' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0012407 pyridoxal phosphate-responsive seizures 'pyridoxal phosphate-responsive seizures' SubClassOf 'monogenic epilepsy' 'pyridoxal phosphate-responsive seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012289 myofibrillar myopathy 5 'myofibrillar myopathy 5' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012143 hereditary cryohydrocytosis with reduced stomatin 'hereditary cryohydrocytosis with reduced stomatin' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012192 permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome 'permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0036193 parkinsonism with polyneuropathy 'parkinsonism with polyneuropathy' SubClassOf 'genetic disorder' 'parkinsonism with polyneuropathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012033 bradyopsia 'bradyopsia' SubClassOf 'genetic disorder' 'bradyopsia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0012061 familial sick sinus syndrome 'familial sick sinus syndrome' SubClassOf 'genetic disorder' 'familial sick sinus syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_0009904 Lopes-Maciel-Rodan syndrome 'Lopes-Maciel-Rodan syndrome' SubClassOf 'nervous system disease' 'Lopes-Maciel-Rodan syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0020660 prostate-specific antigen measurement 'prostate-specific antigen measurement' SubClassOf 'protein measurement' 'prostate-specific antigen measurement' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/UBERON_0001184 renal artery 'renal artery' SubClassOf 'part of' some 'abdominal aorta' http://purl.obolibrary.org/obo/MONDO_0007113 Angelman syndrome 'Angelman syndrome' SubClassOf 'nervous system disease' 'Angelman syndrome' SubClassOf 'genetic disorder' 'Angelman syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007187 nevoid basal cell carcinoma syndrome 'nevoid basal cell carcinoma syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007194 familial bicuspid aortic valve 'familial bicuspid aortic valve' SubClassOf 'genetic disorder' 'familial bicuspid aortic valve' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0012986 bilateral parasagittal parieto-occipital polymicrogyria 'bilateral parasagittal parieto-occipital polymicrogyria' SubClassOf 'genetic disorder' 'bilateral parasagittal parieto-occipital polymicrogyria' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/UBERON_0001323 tibial nerve 'tibial nerve' SubClassOf 'part of' some 'sciatic nerve' http://purl.obolibrary.org/obo/MONDO_0012714 early-onset myopathy with fatal cardiomyopathy 'early-onset myopathy with fatal cardiomyopathy' SubClassOf 'neuromuscular disease' 'early-onset myopathy with fatal cardiomyopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://www.orpha.net/ORDO/Orphanet_183509 Rare genetic headache 'Rare genetic headache' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.orpha.net/ORDO/Orphanet_183521 Rare genetic movement disorder 'Rare genetic movement disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017306 disorder of phenylalanine metabolism 'disorder of phenylalanine metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0017307 disorder of tyrosine metabolism 'disorder of tyrosine metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0017317 phakomatosis pigmentokeratotica 'phakomatosis pigmentokeratotica' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017355 inborn disorder of proline metabolism 'inborn disorder of proline metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0017356 inborn disorder of ornithine metabolism 'inborn disorder of ornithine metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0017350 inborn disorder of tryptophan metabolism 'inborn disorder of tryptophan metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0007846 KBG syndrome 'KBG syndrome' SubClassOf 'genetic disorder' 'KBG syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0032814 microangiopathy and leukoencephalopathy, pontine, autosomal dominant 'microangiopathy and leukoencephalopathy, pontine, autosomal dominant' SubClassOf 'genetic disorder' 'microangiopathy and leukoencephalopathy, pontine, autosomal dominant' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007732 Holt-Oram syndrome 'Holt-Oram syndrome' SubClassOf 'heart disease' 'Holt-Oram syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/HP_0025428 Bronchospasm 'Bronchospasm' SubClassOf 'Abnormality of the respiratory system' 'Bronchospasm' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/UBERON_0001772 corneal epithelium 'corneal epithelium' SubClassOf 'part of' some 'cornea' http://purl.obolibrary.org/obo/MONDO_0007626 familial congenital palsy of trochlear nerve 'familial congenital palsy of trochlear nerve' SubClassOf 'genetic disorder' 'familial congenital palsy of trochlear nerve' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007656 Gerstmann-Straussler-Scheinker syndrome 'Gerstmann-Straussler-Scheinker syndrome' SubClassOf 'genetic disorder' 'Gerstmann-Straussler-Scheinker syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007688 Myhre syndrome 'Myhre syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007537 lateral meningocele syndrome 'lateral meningocele syndrome' SubClassOf 'genetic disorder' 'lateral meningocele syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0003857 arthrogryposis 'arthrogryposis' SubClassOf 'genetic disorder' 'arthrogryposis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0032594 intellectual developmental disorder and retinitis pigmentosa; IDDRP 'intellectual developmental disorder and retinitis pigmentosa; IDDRP' SubClassOf 'genetic disorder' 'intellectual developmental disorder and retinitis pigmentosa; IDDRP' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007401 craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome 'craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007450 neurohypophyseal diabetes insipidus 'neurohypophyseal diabetes insipidus' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007473 Duane retraction syndrome 'Duane retraction syndrome' SubClassOf 'genetic disorder' 'Duane retraction syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007318 Alagille syndrome 'Alagille syndrome' SubClassOf 'genetic disorder' 'Alagille syndrome' SubClassOf 'heart disease' 'Alagille syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0007316 Chiari malformation type I 'Chiari malformation type I' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0007354 coloboma of optic nerve 'coloboma of optic nerve' SubClassOf 'genetic disorder' 'coloboma of optic nerve' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013099 combined pituitary hormone deficiencies, genetic form 'combined pituitary hormone deficiencies, genetic form' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0003441 dystonic disorder 'dystonic disorder' SubClassOf 'movement disorder' 'dystonic disorder' SubClassOf 'extrapyramidal and movement disease' http://purl.obolibrary.org/obo/MONDO_0042966 inherited mitral valve disease 'inherited mitral valve disease' SubClassOf 'genetic disorder' 'inherited mitral valve disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0017851 erythrokeratodermia variabilis 'erythrokeratodermia variabilis' SubClassOf 'erythrokeratoderma' http://www.ebi.ac.uk/efo/EFO_0004242 obsessive-compulsive disorder 'obsessive-compulsive disorder' SubClassOf 'genetic disorder' 'obsessive-compulsive disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0004266 primary ovarian insufficiency 'primary ovarian insufficiency' SubClassOf 'ovarian disease' 'primary ovarian insufficiency' SubClassOf 'ovarian dysfunction' 'primary ovarian insufficiency' SubClassOf 'ovarian dysfunction' http://purl.obolibrary.org/obo/MONDO_0017824 familial isolated pituitary adenoma 'familial isolated pituitary adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017615 benign familial infantile epilepsy 'benign familial infantile epilepsy' SubClassOf 'monogenic epilepsy' 'benign familial infantile epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017686 inborn aminoacylase deficiency 'inborn aminoacylase deficiency' SubClassOf 'nervous system disease' 'inborn aminoacylase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017681 erythrokeratoderma variabilis progressiva 'erythrokeratoderma variabilis progressiva' SubClassOf 'erythrokeratoderma' 'erythrokeratoderma variabilis progressiva' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/FBbt_00005552 ventral sensory complex primordium 'ventral sensory complex primordium' SubClassOf 'Drosophila developmental tissue' 'ventral sensory complex primordium' SubClassOf 'sensory nervous system primordium' http://www.ebi.ac.uk/efo/EFO_0004540 chronic fatigue syndrome 'chronic fatigue syndrome' SubClassOf 'nervous system disease' 'chronic fatigue syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0017704 familial partial epilepsy 'familial partial epilepsy' SubClassOf 'monogenic epilepsy' 'familial partial epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0008324 response to sulfasalazine 'response to sulfasalazine' SubClassOf 'has_input' some 'sulfasalazine' 'response to sulfasalazine' SubClassOf 'response to xenobiotic stimulus' 'response to sulfasalazine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0008325 response to sotalol 'response to sotalol' SubClassOf 'response to beta blocker' 'response to sotalol' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0008345 response to duloxetine 'response to duloxetine' SubClassOf 'response to serotonin-norephinephrine reuptake inhibitor' 'response to duloxetine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0013907 bilateral generalized polymicrogyria 'bilateral generalized polymicrogyria' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013960 sinoatrial node dysfunction and deafness 'sinoatrial node dysfunction and deafness' SubClassOf 'genetic disorder' 'sinoatrial node dysfunction and deafness' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0037940 inherited auditory system disease 'inherited auditory system disease' SubClassOf 'genetic disorder' 'inherited auditory system disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013988 congenital heart defects, multiple types, 3 'congenital heart defects, multiple types, 3' SubClassOf 'genetic disorder' 'congenital heart defects, multiple types, 3' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0037938 inborn disorder of aspartate family metabolism 'inborn disorder of aspartate family metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0013981 myoclonus, familial 'myoclonus, familial' SubClassOf 'genetic disorder' 'myoclonus, familial' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013875 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome '3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100548 http://purl.obolibrary.org/obo/MONDO_0023224 inherited reflex epilepsy 'inherited reflex epilepsy' SubClassOf 'monogenic epilepsy' 'inherited reflex epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0037870 valine metabolism disease 'valine metabolism disease' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0037871 amino acid metabolism disease 'amino acid metabolism disease' SubClassOf 'disorder of organic acid metabolism' 'amino acid metabolism disease' SubClassOf 'metabolic disease' http://www.ebi.ac.uk/efo/EFO_0008580 response to taxane 'response to taxane' SubClassOf 'response to antimicrotubule agent' 'response to taxane' SubClassOf 'has_input' some 'taxane' 'response to taxane' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0013784 neonatal-onset encephalopathy with rigidity and seizures 'neonatal-onset encephalopathy with rigidity and seizures' SubClassOf 'monogenic epilepsy' http://www.ebi.ac.uk/efo/EFO_0008514 neurofibromatosis 'neurofibromatosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0859390 epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features 'epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0008484 response to carbamazepine 'response to carbamazepine' SubClassOf 'response to anticonvulsant' 'response to carbamazepine' SubClassOf 'is_about' some 'carbamazepine' 'response to carbamazepine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0013640 familial retinal arterial macroaneurysm 'familial retinal arterial macroaneurysm' SubClassOf 'heart disease' 'familial retinal arterial macroaneurysm' SubClassOf 'genetic disorder' 'familial retinal arterial macroaneurysm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 'familial retinal arterial macroaneurysm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013696 chromosome 2p16.3 deletion syndrome 'chromosome 2p16.3 deletion syndrome' SubClassOf 'genetic disorder' 'chromosome 2p16.3 deletion syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013583 occipital pachygyria and polymicrogyria 'occipital pachygyria and polymicrogyria' SubClassOf 'genetic disorder' 'occipital pachygyria and polymicrogyria' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013351 infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly 'infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly' SubClassOf 'genetic disorder' 'infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0013352 intellectual disability-severe speech delay-mild dysmorphism syndrome 'intellectual disability-severe speech delay-mild dysmorphism syndrome' SubClassOf 'genetic disorder' 'intellectual disability-severe speech delay-mild dysmorphism syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/UBERON_0005870 olfactory pit 'olfactory pit' SubClassOf 'part of' some 'anatomical structure' http://purl.obolibrary.org/obo/MONDO_0013208 cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome 'cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008504 supravalvular aortic stenosis 'supravalvular aortic stenosis' SubClassOf 'genetic disorder' 'supravalvular aortic stenosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008501 Sturge-Weber syndrome 'Sturge-Weber syndrome' SubClassOf 'genetic disorder' 'Sturge-Weber syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0002945 familial cardiomyopathy 'familial cardiomyopathy' SubClassOf 'genetic disorder' 'familial cardiomyopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008434 Smith-Magenis syndrome 'Smith-Magenis syndrome' SubClassOf 'genetic disorder' 'Smith-Magenis syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008337 familial pterygium of the conjunctiva 'familial pterygium of the conjunctiva' SubClassOf 'genetic disorder' 'familial pterygium of the conjunctiva' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008209 Char syndrome 'Char syndrome' SubClassOf 'genetic disorder' 'Char syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008201 Perry syndrome 'Perry syndrome' SubClassOf 'genetic disorder' 'Perry syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008222 Andersen-Tawil syndrome 'Andersen-Tawil syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0008108 oculocerebrocutaneous syndrome 'oculocerebrocutaneous syndrome' SubClassOf 'nervous system disease' 'oculocerebrocutaneous syndrome' SubClassOf 'genetic disorder' 'oculocerebrocutaneous syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008179 paroxysmal extreme pain disorder 'paroxysmal extreme pain disorder' SubClassOf 'genetic disorder' 'paroxysmal extreme pain disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008097 linear nevus sebaceous syndrome 'linear nevus sebaceous syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018614 undetermined early-onset epileptic encephalopathy 'undetermined early-onset epileptic encephalopathy' SubClassOf 'monogenic epilepsy' 'undetermined early-onset epileptic encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018507 microcephaly-complex motor and sensory axonal neuropathy syndrome 'microcephaly-complex motor and sensory axonal neuropathy syndrome' SubClassOf 'nervous system disease' 'microcephaly-complex motor and sensory axonal neuropathy syndrome' SubClassOf 'genetic disorder' 'microcephaly-complex motor and sensory axonal neuropathy syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018477 bilirubin encephalopathy 'bilirubin encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018493 malignant hyperthermia of anesthesia 'malignant hyperthermia of anesthesia' SubClassOf 'genetic disorder' 'malignant hyperthermia of anesthesia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0008908 MGAT2-congenital disorder of glycosylation 'MGAT2-congenital disorder of glycosylation' SubClassOf 'heart disease' 'MGAT2-congenital disorder of glycosylation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008915 dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 'dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome' SubClassOf 'heart disease' 'dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome' SubClassOf 'genetic disorder' 'dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008917 heart defects-limb shortening syndrome 'heart defects-limb shortening syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008922 Sengers syndrome 'Sengers syndrome' SubClassOf 'heart disease' 'Sengers syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008965 CHARGE syndrome 'CHARGE syndrome' SubClassOf 'heart disease' 'CHARGE syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0008962 Griscelli syndrome type 1 'Griscelli syndrome type 1' SubClassOf 'nervous system disease' 'Griscelli syndrome type 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008999 Cohen syndrome 'Cohen syndrome' SubClassOf 'genetic disorder' 'Cohen syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018339 PrP systemic amyloidosis 'PrP systemic amyloidosis' SubClassOf 'genetic disorder' 'PrP systemic amyloidosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018343 periodic paralysis with later-onset distal motor neuropathy 'periodic paralysis with later-onset distal motor neuropathy' SubClassOf 'neuromuscular disease' 'periodic paralysis with later-onset distal motor neuropathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0018354 Prader-Willi-like syndrome 'Prader-Willi-like syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/HP_0012328 Cementoma 'Cementoma' SubClassOf 'Abnormality of the digestive system' http://purl.obolibrary.org/obo/MONDO_0008840 ataxia telangiectasia 'ataxia telangiectasia' SubClassOf 'nervous system disease' 'ataxia telangiectasia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008858 Behr syndrome 'Behr syndrome' SubClassOf 'nervous system disease' 'Behr syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018203 LMNA-related cardiocutaneous progeria syndrome 'LMNA-related cardiocutaneous progeria syndrome' SubClassOf 'heart disease' 'LMNA-related cardiocutaneous progeria syndrome' SubClassOf 'genetic disorder' 'LMNA-related cardiocutaneous progeria syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0018214 generalized epilepsy with febrile seizures plus 'generalized epilepsy with febrile seizures plus' SubClassOf 'monogenic epilepsy' 'generalized epilepsy with febrile seizures plus' SubClassOf 'epilepsy' 'generalized epilepsy with febrile seizures plus' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0033864 infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 'infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome' SubClassOf 'genetic disorder' 'infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018257 familial syringomyelia 'familial syringomyelia' SubClassOf 'genetic disorder' 'familial syringomyelia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008759 oxoglutaricaciduria 'oxoglutaricaciduria' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0008758 mitochondrial DNA depletion syndrome 4a 'mitochondrial DNA depletion syndrome 4a' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0018160 hereditary retinoblastoma 'hereditary retinoblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008610 blue color blindness 'blue color blindness' SubClassOf 'genetic disorder' 'blue color blindness' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0008648 ventricular tachycardia, familial 'ventricular tachycardia, familial' SubClassOf 'genetic disorder' 'ventricular tachycardia, familial' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0018045 Hoyeraal-Hreidarsson syndrome 'Hoyeraal-Hreidarsson syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018054 familial atrial fibrillation 'familial atrial fibrillation' SubClassOf 'genetic disorder' 'familial atrial fibrillation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0014320 Bosch-Boonstra-Schaaf optic atrophy syndrome 'Bosch-Boonstra-Schaaf optic atrophy syndrome' SubClassOf 'genetic disorder' 'Bosch-Boonstra-Schaaf optic atrophy syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0007808 response to bortezomib 'response to bortezomib' SubClassOf 'response to antineoplastic agent' 'response to bortezomib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007816 response to trametinib 'response to trametinib' SubClassOf 'response to antineoplastic agent' 'response to trametinib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007815 response to dabrafenib 'response to dabrafenib' SubClassOf 'response to antineoplastic agent' 'response to dabrafenib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007867 response to gefitinib 'response to gefitinib' SubClassOf 'is_about' some 'gefitinib' 'response to gefitinib' SubClassOf 'response to antineoplastic agent' 'response to gefitinib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007866 response to rifampicin 'response to rifampicin' SubClassOf 'is_about' some 'rifampicin' 'response to rifampicin' SubClassOf 'response to antibiotic' 'response to rifampicin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007868 response to erlotinib 'response to erlotinib' SubClassOf 'response to antineoplastic agent' 'response to erlotinib' SubClassOf 'is_about' some 'erlotinib' 'response to erlotinib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007853 response to mercaptopurine 'response to mercaptopurine' SubClassOf 'response to thiopurine' 'response to mercaptopurine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007871 response to escitalopram 'response to escitalopram' SubClassOf 'response to selective serotonin reuptake inhibitor' 'response to escitalopram' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0014419 ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome 'ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome' SubClassOf 'genetic disorder' 'ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014210 intellectual disability-hypotonia-spasticity-sleep disorder syndrome 'intellectual disability-hypotonia-spasticity-sleep disorder syndrome' SubClassOf 'genetic disorder' 'intellectual disability-hypotonia-spasticity-sleep disorder syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014250 familial hyperprolactinemia 'familial hyperprolactinemia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014268 combined immunodeficiency due to OX40 deficiency 'combined immunodeficiency due to OX40 deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to OX40 deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0014263 8q24.3 microdeletion syndrome '8q24.3 microdeletion syndrome' SubClassOf 'heart disease' '8q24.3 microdeletion syndrome' SubClassOf 'genetic disorder' '8q24.3 microdeletion syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0014276 combined immunodeficiency due to CD3gamma deficiency 'combined immunodeficiency due to CD3gamma deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to CD3gamma deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0014300 proximal myopathy with extrapyramidal signs 'proximal myopathy with extrapyramidal signs' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0007779 response to pazopanib 'response to pazopanib' SubClassOf 'response to antineoplastic agent' 'response to pazopanib' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0014314 sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome 'sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome' SubClassOf 'genetic disorder' 'sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014197 combined immunodeficiency due to MALT1 deficiency 'combined immunodeficiency due to MALT1 deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to MALT1 deficiency' SubClassOf 'combined immunodeficiency' http://www.orpha.net/ORDO/Orphanet_271841 Genetic cardiac tumor 'Genetic cardiac tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.orpha.net/ORDO/Orphanet_99095 Gerbode defect 'Gerbode defect' SubClassOf 'heart disease' 'Gerbode defect' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.orpha.net/ORDO/Orphanet_99097 Single ventricular septal defect 'Single ventricular septal defect' SubClassOf 'heart disease' 'Single ventricular septal defect' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.orpha.net/ORDO/Orphanet_99096 Multiple ventricular septal defects 'Multiple ventricular septal defects' SubClassOf 'heart disease' 'Multiple ventricular septal defects' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_0007921 response to nitrofurantoin 'response to nitrofurantoin' SubClassOf 'response to antibiotic' 'response to nitrofurantoin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007925 response to paliperidone 'response to paliperidone' SubClassOf 'response to antipsychotic drug' 'response to paliperidone' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007923 response to terbinafine 'response to terbinafine' SubClassOf 'response to xenobiotic stimulus' 'response to terbinafine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007919 response to diclofenac 'response to diclofenac' SubClassOf 'response to non-steroidal anti-inflammatory' 'response to diclofenac' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007917 response to tetracyclic antidepressant 'response to tetracyclic antidepressant' SubClassOf 'response to antidepressant' 'response to tetracyclic antidepressant' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007943 response to platinum-based neoadjuvant chemotherapy 'response to platinum-based neoadjuvant chemotherapy' SubClassOf 'response to platinum based chemotherapy' 'response to platinum-based neoadjuvant chemotherapy' SubClassOf http://purl.obolibrary.org/obo/OBA_2040037 http://www.ebi.ac.uk/efo/EFO_0007981 response to thiazide 'response to thiazide' SubClassOf 'response to diuretic' 'response to thiazide' SubClassOf 'response to antihypertensive drug' 'response to thiazide' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0004587 hereditary night blindness 'hereditary night blindness' SubClassOf 'genetic disorder' 'hereditary night blindness' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018948 multiminicore myopathy 'multiminicore myopathy' SubClassOf 'genetic disorder' 'multiminicore myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018940 congenital myasthenic syndrome 'congenital myasthenic syndrome' SubClassOf 'genetic disorder' 'congenital myasthenic syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0018953 parietal foramina 'parietal foramina' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018829 familial schizencephaly 'familial schizencephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018838 lissencephaly spectrum disorders 'lissencephaly spectrum disorders' SubClassOf 'genetic disorder' 'lissencephaly spectrum disorders' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0018875 Li-Fraumeni syndrome 'Li-Fraumeni syndrome' SubClassOf 'nervous system disease' 'Li-Fraumeni syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0003105 spina bifida 'spina bifida' SubClassOf 'genetic disorder' 'spina bifida' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0003108 essential tremor 'essential tremor' SubClassOf 'genetic disorder' 'essential tremor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.orpha.net/ORDO/Orphanet_99807 PEHO-like syndrome 'PEHO-like syndrome' SubClassOf 'nervous system disease' 'PEHO-like syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009012 multiple pterygium-malignant hyperthermia syndrome 'multiple pterygium-malignant hyperthermia syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000698 gamma-amino butyric acid metabolism disorder 'gamma-amino butyric acid metabolism disorder' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0010010 Schinzel-Giedion syndrome 'Schinzel-Giedion syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010023 combined immunodeficiency due to ZAP70 deficiency 'combined immunodeficiency due to ZAP70 deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to ZAP70 deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0024560 PDA1 'PDA1' SubClassOf 'genetic disorder' 'PDA1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_0007217 congenital nystagmus 'congenital nystagmus' SubClassOf 'genetic disorder' 'congenital nystagmus' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000453 short QT syndrome 'short QT syndrome' SubClassOf 'genetic disorder' 'short QT syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0000456 cerebral creatine deficiency syndrome 'cerebral creatine deficiency syndrome' SubClassOf 'monogenic epilepsy' 'cerebral creatine deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000465 atrioventricular block 'atrioventricular block' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0024257 hereditary motor neuron disease 'hereditary motor neuron disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0014944 short stature-brachydactyly-obesity-global developmental delay syndrome 'short stature-brachydactyly-obesity-global developmental delay syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000166 encephalopathy, acute, infection-induced 'encephalopathy, acute, infection-induced' SubClassOf 'genetic disorder' 'encephalopathy, acute, infection-induced' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0700117 SLC6A3-related dopamine transporter deficiency syndrome 'SLC6A3-related dopamine transporter deficiency syndrome' SubClassOf 'genetic disorder' 'SLC6A3-related dopamine transporter deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000188 GLUT1 deficiency syndrome 'GLUT1 deficiency syndrome' SubClassOf 'monogenic epilepsy' 'GLUT1 deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014832 intellectual disability, autosomal recessive 53 'intellectual disability, autosomal recessive 53' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0700068 myopathy caused by variation in POMGNT1 'myopathy caused by variation in POMGNT1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014878 patent ductus arteriosus 2 'patent ductus arteriosus 2' SubClassOf 'genetic disorder' 'patent ductus arteriosus 2' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0014881 transketolase deficiency 'transketolase deficiency' SubClassOf 'heart disease' 'transketolase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0024237 inherited neurodegenerative disorder 'inherited neurodegenerative disorder' SubClassOf 'genetic disorder' 'inherited neurodegenerative disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0700002 ATP1A3-associated neurological disorder 'ATP1A3-associated neurological disorder' SubClassOf 'genetic disorder' 'ATP1A3-associated neurological disorder' SubClassOf 'nervous system disease' 'ATP1A3-associated neurological disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014746 SLC39A8-CDG 'SLC39A8-CDG' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000137 leukoencephalopathy, megalencephalic 'leukoencephalopathy, megalencephalic' SubClassOf 'genetic disorder' 'leukoencephalopathy, megalencephalic' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014773 cardiac anomalies - developmental delay - facial dysmorphism syndrome 'cardiac anomalies - developmental delay - facial dysmorphism syndrome' SubClassOf 'heart disease' 'cardiac anomalies - developmental delay - facial dysmorphism syndrome' SubClassOf 'genetic disorder' 'cardiac anomalies - developmental delay - facial dysmorphism syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 'cardiac anomalies - developmental delay - facial dysmorphism syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014784 severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome 'severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome' SubClassOf 'heart disease' 'severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0014787 severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome 'severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome' SubClassOf 'genetic disorder' 'severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0007676 response to zileuton 'response to zileuton' SubClassOf 'response to xenobiotic stimulus' 'response to zileuton' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007612 response to montelukast 'response to montelukast' SubClassOf 'response to xenobiotic stimulus' 'response to montelukast' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007647 response to vancomycin 'response to vancomycin' SubClassOf 'response to antibiotic' 'response to vancomycin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007661 response to lamotrigine 'response to lamotrigine' SubClassOf 'response to anticonvulsant' 'response to lamotrigine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007662 response to triptolide 'response to triptolide' SubClassOf 'response to xenobiotic stimulus' 'response to triptolide' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0007592 response to bleomycin 'response to bleomycin' SubClassOf 'is_about' some 'bleomycin' 'response to bleomycin' SubClassOf 'response to antineoplastic agent' 'response to bleomycin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0014546 myopathy due to calsequestrin and SERCA1 protein overload 'myopathy due to calsequestrin and SERCA1 protein overload' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014552 lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 'lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014559 progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 'progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0014558 autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 'autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome' SubClassOf 'heart disease' 'autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0010826 childhood absence epilepsy 'childhood absence epilepsy' SubClassOf 'monogenic epilepsy' 'childhood absence epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009856 Peters plus syndrome 'Peters plus syndrome' SubClassOf 'heart disease' 'Peters plus syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_1001510 specific language impairment 'specific language impairment' SubClassOf 'genetic disorder' 'specific language impairment' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019228 inborn disorder of histidine metabolism 'inborn disorder of histidine metabolism' SubClassOf 'amino acid metabolism disease' 'inborn disorder of histidine metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0019239 inborn disorder of serine family metabolism 'inborn disorder of serine family metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0019242 inborn disorder of branched-chain amino acid metabolism 'inborn disorder of branched-chain amino acid metabolism' SubClassOf 'disorder of organic acid metabolism' http://purl.obolibrary.org/obo/MONDO_0020246 inherited vitreoretinopathy 'inherited vitreoretinopathy' SubClassOf 'genetic disorder' 'inherited vitreoretinopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0020290 familial atrioventricular septal defect 'familial atrioventricular septal defect' SubClassOf 'genetic disorder' 'familial atrioventricular septal defect' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0009719 familial atrial myxoma 'familial atrial myxoma' SubClassOf 'genetic disorder' 'familial atrial myxoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0009714 myosclerosis 'myosclerosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009722 Bailey-Bloch congenital myopathy 'Bailey-Bloch congenital myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010711 TARP syndrome 'TARP syndrome' SubClassOf 'genetic disorder' 'TARP syndrome' SubClassOf 'heart disease' 'TARP syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/UBERON_0003684 abdominal cavity 'abdominal cavity' SubClassOf 'part of' some 'abdomen' http://purl.obolibrary.org/obo/MONDO_0010753 cardiac valvular dysplasia, X-linked 'cardiac valvular dysplasia, X-linked' SubClassOf 'genetic disorder' 'cardiac valvular dysplasia, X-linked' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0019118 inherited retinal dystrophy 'inherited retinal dystrophy' SubClassOf 'genetic disorder' 'inherited retinal dystrophy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010794 NARP syndrome 'NARP syndrome' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0020135 pontocerebellar hypoplasia 'pontocerebellar hypoplasia' SubClassOf 'genetic disorder' 'pontocerebellar hypoplasia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0020121 muscular dystrophy 'muscular dystrophy' SubClassOf 'neuromuscular disease' 'muscular dystrophy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0020127 hereditary peripheral neuropathy 'hereditary peripheral neuropathy' SubClassOf 'genetic disorder' 'hereditary peripheral neuropathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0019171 familial long QT syndrome 'familial long QT syndrome' SubClassOf 'genetic disorder' 'familial long QT syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0019169 pyruvate dehydrogenase deficiency 'pyruvate dehydrogenase deficiency' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0019197 folinic acid-responsive seizures 'folinic acid-responsive seizures' SubClassOf 'monogenic epilepsy' 'folinic acid-responsive seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009666 holocarboxylase synthetase deficiency 'holocarboxylase synthetase deficiency' SubClassOf 'monogenic epilepsy' 'holocarboxylase synthetase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009665 biotinidase deficiency 'biotinidase deficiency' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0009664 mulibrey nanism 'mulibrey nanism' SubClassOf 'bearer_of' some 'rare' http://purl.obolibrary.org/obo/MONDO_0019053 peroxisomal disease 'peroxisomal disease' SubClassOf 'monogenic epilepsy' 'peroxisomal disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019064 hereditary spastic paraplegia 'hereditary spastic paraplegia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0020074 progressive myoclonus epilepsy 'progressive myoclonus epilepsy' SubClassOf 'monogenic epilepsy' 'progressive myoclonus epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019078 Ritscher-Schinzel syndrome 'Ritscher-Schinzel syndrome' SubClassOf 'genetic disorder' 'Ritscher-Schinzel syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001485 acromegaly 'acromegaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009511 Larsen-like syndrome, B3GAT3 type 'Larsen-like syndrome, B3GAT3 type' SubClassOf 'heart disease' 'Larsen-like syndrome, B3GAT3 type' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0010514 combined immunodeficiency due to moesin deficiency 'combined immunodeficiency due to moesin deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to moesin deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0010542 dilated cardiomyopathy 3B 'dilated cardiomyopathy 3B' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009578 neurocutaneous melanocytosis 'neurocutaneous melanocytosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/GO_0072718 response to cisplatin 'response to cisplatin' SubClassOf 'response to platinum based chemotherapy' 'response to cisplatin' SubClassOf http://purl.obolibrary.org/obo/OBA_2040037 http://purl.obolibrary.org/obo/MONDO_0010441 CK syndrome 'CK syndrome' SubClassOf 'genetic disorder' 'CK syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001040 meningococcal meningitis 'meningococcal meningitis' SubClassOf 'meningococcal infection' http://www.ebi.ac.uk/efo/EFO_1001210 tethered spinal cord syndrome 'tethered spinal cord syndrome' SubClassOf 'genetic disorder' 'tethered spinal cord syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000904 complex cortical dysplasia with other brain malformations 'complex cortical dysplasia with other brain malformations' SubClassOf 'genetic disorder' 'complex cortical dysplasia with other brain malformations' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000995 familial periodic paralysis 'familial periodic paralysis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010327 HSD10 mitochondrial disease 'HSD10 mitochondrial disease' SubClassOf 'nervous system disease' 'HSD10 mitochondrial disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009341 Mowat-Wilson syndrome 'Mowat-Wilson syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010397 severe neonatal-onset encephalopathy with microcephaly 'severe neonatal-onset encephalopathy with microcephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001190 splenic infarction 'splenic infarction' SubClassOf 'digestive system disease' http://www.orpha.net/ORDO/Orphanet_357027 Familial retinoblastoma 'Familial retinoblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.orpha.net/ORDO/Orphanet_113 Bazex-Dupré-Christol syndrome 'Bazex-Dupré-Christol syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000819 anencephaly 'anencephaly' SubClassOf 'genetic disorder' 'anencephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010221 CHIME syndrome 'CHIME syndrome' SubClassOf 'heart disease' 'CHIME syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0010243 X-linked immunoneurologic disorder 'X-linked immunoneurologic disorder' SubClassOf 'nervous system disease' 'X-linked immunoneurologic disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009281 glutaryl-CoA dehydrogenase deficiency 'glutaryl-CoA dehydrogenase deficiency' SubClassOf 'nervous system disease' 'glutaryl-CoA dehydrogenase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0034099 SYNGAP1-related developmental and epileptic encephalopathy 'SYNGAP1-related developmental and epileptic encephalopathy' SubClassOf 'monogenic epilepsy' 'SYNGAP1-related developmental and epileptic encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001010 Landau-Kleffner syndrome 'Landau-Kleffner syndrome' SubClassOf 'monogenic epilepsy' 'Landau-Kleffner syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000700 familial hemiplegic migraine 'familial hemiplegic migraine' SubClassOf 'genetic disorder' 'familial hemiplegic migraine' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0000723 stutter disorder 'stutter disorder' SubClassOf 'genetic disorder' 'stutter disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009131 Riley-Day syndrome 'Riley-Day syndrome' SubClassOf 'genetic disorder' 'Riley-Day syndrome' SubClassOf 'nervous system disease' 'Riley-Day syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009159 Ehlers-Danlos syndrome, cardiac valvular type 'Ehlers-Danlos syndrome, cardiac valvular type' SubClassOf 'heart disease' 'Ehlers-Danlos syndrome, cardiac valvular type' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0009162 Ellis-van Creveld syndrome 'Ellis-van Creveld syndrome' SubClassOf 'heart disease' 'Ellis-van Creveld syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0010159 mismatch repair cancer syndrome 1 'mismatch repair cancer syndrome 1' SubClassOf 'nervous system disease' 'mismatch repair cancer syndrome 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010176 orofaciodigital syndrome type 6 'orofaciodigital syndrome type 6' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0005301 multiple sclerosis 'multiple sclerosis' SubClassOf 'demyelinating disease' 'multiple sclerosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0020800 http://purl.obolibrary.org/obo/MONDO_0020831 congenital vertebral-cardiac-renal anomalies syndrome 'congenital vertebral-cardiac-renal anomalies syndrome' SubClassOf 'heart disease' 'congenital vertebral-cardiac-renal anomalies syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0044807 inherited dystonia 'inherited dystonia' SubClassOf 'genetic disorder' 'inherited dystonia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.orpha.net/ORDO/Orphanet_661 Ondine syndrome 'Ondine syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0020745 ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome 'ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0044725 combined immunodeficiency due to GINS1 deficiency 'combined immunodeficiency due to GINS1 deficiency' SubClassOf 'immunodeficiency disease' 'combined immunodeficiency due to GINS1 deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0005180 Parkinson disease 'Parkinson disease' SubClassOf 'genetic disorder' 'Parkinson disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0020627 epileptic encephalopathy, infantile or early childhood 'epileptic encephalopathy, infantile or early childhood' SubClassOf 'monogenic epilepsy' 'epileptic encephalopathy, infantile or early childhood' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001918 specific phobia 'specific phobia' SubClassOf 'genetic disorder' 'specific phobia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001926 pathological gambling 'pathological gambling' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019502 autosomal recessive non-syndromic intellectual disability 'autosomal recessive non-syndromic intellectual disability' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019490 progressive familial heart block 'progressive familial heart block' SubClassOf 'genetic disorder' 'progressive familial heart block' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0020496 familial porencephaly 'familial porencephaly' SubClassOf 'genetic disorder' 'familial porencephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0020485 King-Denborough syndrome 'King-Denborough syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009934 alveolar capillary dysplasia with misalignment of pulmonary veins 'alveolar capillary dysplasia with misalignment of pulmonary veins' SubClassOf 'genetic disorder' 'alveolar capillary dysplasia with misalignment of pulmonary veins' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0009945 pyridoxine-dependent epilepsy 'pyridoxine-dependent epilepsy' SubClassOf 'monogenic epilepsy' 'pyridoxine-dependent epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_1001857 Takayasu arteritis 'Takayasu arteritis' SubClassOf 'nervous system disease' 'Takayasu arteritis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009966 NPHP3-related Meckel-like syndrome 'NPHP3-related Meckel-like syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0009974 familial hemophagocytic lymphohistiocytosis type 1 'familial hemophagocytic lymphohistiocytosis type 1' SubClassOf 'nervous system disease' 'familial hemophagocytic lymphohistiocytosis type 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0010977 Brody myopathy 'Brody myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0044304 hyperphenylalaninemia due to DNAJC12 deficiency 'hyperphenylalaninemia due to DNAJC12 deficiency' SubClassOf 'inborn disorder of amino acid and other organic acid metabolism' 'hyperphenylalaninemia due to DNAJC12 deficiency' SubClassOf 'inborn errors of metabolism' http://purl.obolibrary.org/obo/MONDO_0020341 periventricular nodular heterotopia 'periventricular nodular heterotopia' SubClassOf 'genetic disorder' 'periventricular nodular heterotopia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0019375 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome 'megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015653 monogenic epilepsy 'monogenic epilepsy' SubClassOf 'genetic disorder' 'monogenic epilepsy' EquivalentTo 'epilepsy' and ('bearer_of' some 'inherited') http://www.ebi.ac.uk/efo/EFO_0006518 response to losartan 'response to losartan' SubClassOf 'is_about' some 'losartan' 'response to losartan' SubClassOf 'response to antihypertensive drug' 'response to losartan' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0015739 adult-onset nemaline myopathy 'adult-onset nemaline myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015738 childhood-onset nemaline myopathy 'childhood-onset nemaline myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015737 typical nemaline myopathy 'typical nemaline myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015735 severe congenital nemaline myopathy 'severe congenital nemaline myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015547 hereditary dementia 'hereditary dementia' SubClassOf 'genetic disorder' 'hereditary dementia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015597 pustulosis palmaris et plantaris 'pustulosis palmaris et plantaris' SubClassOf 'dermatitis' 'pustulosis palmaris et plantaris' SubClassOf 'psoriasis' http://purl.obolibrary.org/obo/MONDO_0040566 inherited glutathione metabolism disease 'inherited glutathione metabolism disease' SubClassOf 'sulfur metabolism disease' http://purl.obolibrary.org/obo/MONDO_0015609 advanced sleep phase syndrome 'advanced sleep phase syndrome' SubClassOf 'genetic disorder' 'advanced sleep phase syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://www.ebi.ac.uk/efo/EFO_0006790 cerebral amyloid angiopathy 'cerebral amyloid angiopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0015263 Brugada syndrome 'Brugada syndrome' SubClassOf 'genetic disorder' 'Brugada syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_0006905 response to abacavir 'response to abacavir' SubClassOf 'response to reverse transcriptase inhibitor' 'response to abacavir' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006904 response to efavirenz 'response to efavirenz' SubClassOf 'response to reverse transcriptase inhibitor' 'response to efavirenz' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006950 response to vincristine 'response to vincristine' SubClassOf 'response to antimicrotubule agent' 'response to vincristine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006954 response to triamcinolone acetonide 'response to triamcinolone acetonide' SubClassOf 'response to xenobiotic stimulus' 'response to triamcinolone acetonide' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006998 response to stavudine 'response to stavudine' SubClassOf 'response to reverse transcriptase inhibitor' 'response to stavudine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006996 response to homoharringtonine 'response to homoharringtonine' SubClassOf 'response to antineoplastic agent' 'response to homoharringtonine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006816 response to heparin 'response to heparin' SubClassOf 'response to anticoagulant' 'response to heparin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006862 Meniere disease 'Meniere disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/OBA_2050333 trait in response to oxaliplatin 'trait in response to oxaliplatin' SubClassOf 'response to platinum based chemotherapy' 'trait in response to oxaliplatin' SubClassOf http://purl.obolibrary.org/obo/OBA_2040037 http://purl.obolibrary.org/obo/MONDO_0030512 spastic paraplegia 85, autosomal recessive 'spastic paraplegia 85, autosomal recessive' SubClassOf 'hereditary spastic paraplegia' 'spastic paraplegia 85, autosomal recessive' SubClassOf 'complex hereditary spastic paraplegia' http://www.orpha.net/ORDO/Orphanet_98543 Metabolic disease with dementia 'Metabolic disease with dementia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011376 ventricular fibrillation, paroxysmal familial, type 1 'ventricular fibrillation, paroxysmal familial, type 1' SubClassOf 'genetic disorder' 'ventricular fibrillation, paroxysmal familial, type 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://purl.obolibrary.org/obo/MONDO_0011178 infantile convulsions and choreoathetosis 'infantile convulsions and choreoathetosis' SubClassOf 'monogenic epilepsy' http://purl.obolibrary.org/obo/MONDO_0011184 childhood apraxia of speech 'childhood apraxia of speech' SubClassOf 'genetic disorder' 'childhood apraxia of speech' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0035133 PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome 'PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome' SubClassOf 'genetic disorder' 'PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011213 Pierpont syndrome 'Pierpont syndrome' SubClassOf 'genetic disorder' 'Pierpont syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011240 megalencephaly-capillary malformation-polymicrogyria syndrome 'megalencephaly-capillary malformation-polymicrogyria syndrome' SubClassOf 'genetic disorder' 'megalencephaly-capillary malformation-polymicrogyria syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011053 intellectual disability-sparse hair-brachydactyly syndrome 'intellectual disability-sparse hair-brachydactyly syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011076 myofibrillar myopathy 1 'myofibrillar myopathy 1' SubClassOf 'neuromuscular disease' 'myofibrillar myopathy 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100546 http://purl.obolibrary.org/obo/MONDO_0011090 isolated hereditary congenital facial paralysis 'isolated hereditary congenital facial paralysis' SubClassOf 'genetic disorder' 'isolated hereditary congenital facial paralysis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0001734 tuberous sclerosis 'tuberous sclerosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/MONDO_0011142 Ehlers-Danlos syndrome, musculocontractural type 'Ehlers-Danlos syndrome, musculocontractural type' SubClassOf 'heart disease' 'Ehlers-Danlos syndrome, musculocontractural type' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.orpha.net/ORDO/Orphanet_98685 Oculomotor palsy 'Oculomotor palsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100545 http://purl.obolibrary.org/obo/OBA_2040412 level of prostate-specific antigen in blood serum 'level of prostate-specific antigen in blood serum' SubClassOf 'inheres in' some ('prostate-specific antigen' and ('part of' some 'anatomical entity')) 'level of prostate-specific antigen in blood serum' SubClassOf 'amount' 'level of prostate-specific antigen in blood serum' SubClassOf http://purl.obolibrary.org/obo/OBA_2050200 http://purl.obolibrary.org/obo/MONDO_0001422 primary aldosteronism 'primary aldosteronism' SubClassOf 'adrenal gland disease' 'primary aldosteronism' SubClassOf 'hyperaldosteronism' http://www.orpha.net/ORDO/Orphanet_98054 Rare genetic cardiac disease 'Rare genetic cardiac disease' SubClassOf 'heart disease' 'Rare genetic cardiac disease' SubClassOf 'genetic disorder' 'Rare genetic cardiac disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100547 http://www.ebi.ac.uk/efo/EFO_0006345 response to phenytoin 'response to phenytoin' SubClassOf 'response to anticonvulsant' 'response to phenytoin' SubClassOf 'is_about' some 'phenytoin' 'response to phenytoin' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006314 response to high-dose melphalan 'response to high-dose melphalan' SubClassOf 'response to antineoplastic agent' 'response to high-dose melphalan' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006317 response to thiopurine 'response to thiopurine' SubClassOf 'response to xenobiotic stimulus' 'response to thiopurine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006330 response to buspirone 'response to buspirone' SubClassOf 'response to antidepressant' 'response to buspirone' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006337 response to allopurinol 'response to allopurinol' SubClassOf 'response to xenobiotic stimulus' 'response to allopurinol' SubClassOf 'is_about' some 'allopurinol' 'response to allopurinol' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006326 response to bupropion 'response to bupropion' SubClassOf 'response to norepinephrine-dopamine reuptake inhibitor' 'response to bupropion' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006329 response to citalopram 'response to citalopram' SubClassOf 'response to selective serotonin reuptake inhibitor' 'response to citalopram' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_0006328 response to venlafaxine 'response to venlafaxine' SubClassOf 'response to serotonin-norephinephrine reuptake inhibitor' 'response to venlafaxine' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/OBA_2040004 trait in response to erlotinib 'trait in response to erlotinib' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040005 trait in response to efavirenz 'trait in response to efavirenz' SubClassOf 'response to antiviral drug' http://purl.obolibrary.org/obo/OBA_2040001 trait in response to zileuton 'trait in response to zileuton' SubClassOf 'trait in response to antirheumatic drug' http://purl.obolibrary.org/obo/OBA_2040037 trait in response to platinum 'trait in response to platinum' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040039 trait in response to carbamazepine 'trait in response to carbamazepine' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040030 trait in response to ethanol 'trait in response to ethanol' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040033 trait in response to bupropion 'trait in response to bupropion' SubClassOf 'response to antidepressant' http://purl.obolibrary.org/obo/OBA_2040034 trait in response to buspirone 'trait in response to buspirone' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040024 trait in response to vincristine 'trait in response to vincristine' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040025 trait in response to cytarabine 'trait in response to cytarabine' SubClassOf 'response to immunosuppressant' 'trait in response to cytarabine' SubClassOf 'response to antimetabolite' 'trait in response to cytarabine' SubClassOf 'response to antineoplastic agent' http://purl.obolibrary.org/obo/OBA_2040028 trait in response to melphalan 'trait in response to melphalan' SubClassOf 'response to antineoplastic agent' 'trait in response to melphalan' SubClassOf 'response to immunosuppressant' http://purl.obolibrary.org/obo/OBA_2040029 trait in response to silicon dioxide 'trait in response to silicon dioxide' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040021 trait in response to vancomycin 'trait in response to vancomycin' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040022 trait in response to rifampicin 'trait in response to rifampicin' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040023 trait in response to heparin 'trait in response to heparin' SubClassOf 'response to anticoagulant' http://purl.obolibrary.org/obo/OBA_2040015 trait in response to bleomycin 'trait in response to bleomycin' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040083 trait in response to thiazide 'trait in response to thiazide' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040085 trait in response to mercaptopurine 'trait in response to mercaptopurine' SubClassOf 'response to antimetabolite' http://purl.obolibrary.org/obo/OBA_2040086 trait in response to montelukast 'trait in response to montelukast' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040089 trait in response to tetracyclic antidepressant 'trait in response to tetracyclic antidepressant' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040091 trait in response to bortezomib 'trait in response to bortezomib' SubClassOf 'response to protease inhibitor' http://purl.obolibrary.org/obo/OBA_2040079 trait in response to gefitinib 'trait in response to gefitinib' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040071 trait in response to abacavir 'trait in response to abacavir' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040073 trait in response to paclitaxel 'trait in response to paclitaxel' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040075 trait in response to diclofenac 'trait in response to diclofenac' SubClassOf 'trait in response to antirheumatic drug' http://purl.obolibrary.org/obo/OBA_2040067 trait in response to allopurinol 'trait in response to allopurinol' SubClassOf 'trait in response to antirheumatic drug' http://purl.obolibrary.org/obo/OBA_2040057 trait in response to citalopram 'trait in response to citalopram' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040051 trait in response to thiopurine 'trait in response to thiopurine' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040054 trait in response to taxane 'trait in response to taxane' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040055 trait in response to escitalopram 'trait in response to escitalopram' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040056 trait in response to duloxetine 'trait in response to duloxetine' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040093 trait in response to hydrochlorothiazide 'trait in response to hydrochlorothiazide' SubClassOf 'trait in response to thiazide' http://purl.obolibrary.org/obo/CHEBI_5778 hydrochlorothiazide 'hydrochlorothiazide' SubClassOf 'thiazide' http://purl.obolibrary.org/obo/CHEBI_80630 irinotecan 'irinotecan' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_9943 venlafaxine 'venlafaxine' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/CHEBI_70746 dabigatran etexilate 'dabigatran etexilate' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_9448 terbinafine 'terbinafine' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/CHEBI_9747 Triptolide 'Triptolide' SubClassOf 'isoprenoid' 'Triptolide' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/MONDO_0100541 GATA5-related congenital heart defects 'GATA5-related congenital heart defects' SubClassOf 'congenital heart disease' http://purl.obolibrary.org/obo/MONDO_0100545 hereditary neurological disease 'hereditary neurological disease' SubClassOf 'genetic disorder' 'hereditary neurological disease' SubClassOf 'nervous system disease' 'hereditary neurological disease' EquivalentTo 'nervous system disease' and ('bearer_of' some 'inherited') http://purl.obolibrary.org/obo/MONDO_0100546 hereditary neuromuscular disease 'hereditary neuromuscular disease' SubClassOf 'hereditary neurological disease' 'hereditary neuromuscular disease' SubClassOf 'neuromuscular disease' 'hereditary neuromuscular disease' EquivalentTo 'neuromuscular disease' and ('bearer_of' some 'inherited') http://purl.obolibrary.org/obo/MONDO_0100547 cardiogenetic disease 'cardiogenetic disease' SubClassOf 'heart disease' 'cardiogenetic disease' SubClassOf 'genetic disorder' 'cardiogenetic disease' EquivalentTo 'heart disease' and ('bearer_of' some 'inherited') http://purl.obolibrary.org/obo/MONDO_0100548 SERAC1-related neurological disorder 'SERAC1-related neurological disorder' SubClassOf 'hereditary neurological disease' http://purl.obolibrary.org/obo/CHEBI_50730 montelukast 'montelukast' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_50940 tetracyclic antidepressant 'tetracyclic antidepressant' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_50264 thiazide 'thiazide' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_71219 pazopanib 'pazopanib' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_71418 triamcinolone acetonide 'triamcinolone acetonide' SubClassOf 'organic heterocyclic compound' 'triamcinolone acetonide' SubClassOf 'steroid hormone' http://purl.obolibrary.org/obo/CHEBI_119486 efavirenz 'efavirenz' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_75045 dabrafenib 'dabrafenib' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_75998 trametinib 'trametinib' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_36796 duloxetine 'duloxetine' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_71019 omacetaxine mepesuccinate 'omacetaxine mepesuccinate' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/MONDO_0859689 hepatobiliary benign neoplasm 'hepatobiliary benign neoplasm' SubClassOf 'benign digestive system neoplasm' http://purl.obolibrary.org/obo/CHEBI_3219 bupropion 'bupropion' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/CHEBI_3223 buspirone 'buspirone' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_82978 paliperidone 'paliperidone' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/HP_0012760 Reduced social reciprocity 'Reduced social reciprocity' SubClassOf 'Atypical behavior' http://www.ebi.ac.uk/efo/EFO_0022597 aging 'aging' SubClassOf 'developmental process' http://purl.obolibrary.org/obo/CHEBI_6367 lamotrigine 'lamotrigine' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_30563 silicon dioxide 'silicon dioxide' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/MONDO_0020800 demyelinating disease of central nervous system 'demyelinating disease of central nervous system' SubClassOf 'demyelinating disease' http://purl.obolibrary.org/obo/CHEBI_421707 abacavir 'abacavir' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_28876 melphalan 'melphalan' SubClassOf 'amino acid' http://purl.obolibrary.org/obo/CHEBI_28304 heparin 'heparin' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/OBA_2050200 prostate specific antigen amount 'prostate specific antigen amount' SubClassOf 'amount' 'prostate specific antigen amount' SubClassOf 'inheres in' some ('prostate-specific antigen' and ('part of' some 'anatomical entity')) 'prostate specific antigen amount' EquivalentTo 'amount' and ('inheres in' some ('prostate-specific antigen' and ('part of' some 'anatomical entity'))) http://purl.obolibrary.org/obo/CHEBI_10112 zileuton 'zileuton' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/CHEBI_63622 sotalol 'sotalol' SubClassOf 'chemical entity' http://purl.obolibrary.org/obo/CHEBI_63581 stavudine 'stavudine' SubClassOf 'organic heterocyclic compound' http://purl.obolibrary.org/obo/OBA_2040128 trait in response to irinotecan 'trait in response to irinotecan' SubClassOf 'response to antineoplastic agent' http://purl.obolibrary.org/obo/OBA_2040122 trait in response to trametinib 'trait in response to trametinib' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040121 trait in response to dabrafenib 'trait in response to dabrafenib' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040115 trait in response to omacetaxine mepesuccinate 'trait in response to omacetaxine mepesuccinate' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040114 trait in response to dabigatran etexilate 'trait in response to dabigatran etexilate' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040117 trait in response to pazopanib 'trait in response to pazopanib' SubClassOf 'response to antineoplastic agent' http://purl.obolibrary.org/obo/OBA_2040119 trait in response to triamcinolone acetonide 'trait in response to triamcinolone acetonide' SubClassOf 'response to glucocorticoid' http://purl.obolibrary.org/obo/OBA_2040118 trait in response to nitrofurantoin 'trait in response to nitrofurantoin' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040102 trait in response to sotalol 'trait in response to sotalol' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040101 trait in response to stavudine 'trait in response to stavudine' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040104 trait in response to lamotrigine 'trait in response to lamotrigine' SubClassOf 'response to calcium channel blocker' http://purl.obolibrary.org/obo/OBA_2040108 trait in response to losartan 'trait in response to losartan' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040140 trait in response to Triptolide 'trait in response to Triptolide' SubClassOf 'response to stimulus' http://purl.obolibrary.org/obo/OBA_2040141 trait in response to venlafaxine 'trait in response to venlafaxine' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040137 trait in response to sulfasalazine 'trait in response to sulfasalazine' SubClassOf 'trait in response to antirheumatic drug' http://purl.obolibrary.org/obo/OBA_2040139 trait in response to terbinafine 'trait in response to terbinafine' SubClassOf 'response to xenobiotic stimulus' http://purl.obolibrary.org/obo/OBA_2040130 trait in response to phenytoin 'trait in response to phenytoin' SubClassOf 'response to anticonvulsant' http://purl.obolibrary.org/obo/OBA_2040133 trait in response to prednisolone 'trait in response to prednisolone' SubClassOf 'response to glucocorticoid' http://purl.obolibrary.org/obo/OBA_2040132 trait in response to paliperidone 'trait in response to paliperidone' SubClassOf 'response to antipsychotic drug'