79 19 6 http://purl.obolibrary.org/obo/MONDO_0033548 myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies 'myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies' SubClassOf 'bearer_of' some 'congenital' 'myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies' SubClassOf 'genetic disorder' 'myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies' SubClassOf 'congenital myopathy' http://www.ebi.ac.uk/efo/EFO_0000668 preeclampsia 'preeclampsia' SubClassOf 'genetic hypertension' 'preeclampsia' SubClassOf 'bearer_of' some 'rare' 'preeclampsia' SubClassOf 'genetic disorder' http://purl.obolibrary.org/obo/MONDO_0008323 Liddle syndrome 'Liddle syndrome' SubClassOf 'genetic hypertension' 'Liddle syndrome' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/CHEBI_33568 adrenaline 'adrenaline' SubClassOf 'phenols' 'adrenaline' SubClassOf 'chemical entity' http://www.ebi.ac.uk/efo/EFO_0000717 systemic scleroderma 'systemic scleroderma' SubClassOf 'autoimmune cardiomyopathy' 'systemic scleroderma' SubClassOf 'secondary glomerular disease' 'systemic scleroderma' SubClassOf 'familial restrictive cardiomyopathy' 'systemic scleroderma' SubClassOf 'respiratory system disease' 'systemic scleroderma' SubClassOf 'Non-familial restrictive cardiomyopathy' 'systemic scleroderma' SubClassOf 'respiratory system disease' http://purl.obolibrary.org/obo/MONDO_0008048 autosomal dominant centronuclear myopathy 'autosomal dominant centronuclear myopathy' SubClassOf 'centronuclear myopathy' 'autosomal dominant centronuclear myopathy' SubClassOf 'centronuclear myopathy' http://purl.obolibrary.org/obo/MONDO_0060627 glycosylphosphatidylinositol biosynthesis defect 15 'glycosylphosphatidylinositol biosynthesis defect 15' SubClassOf 'congenital nervous system disorder' 'glycosylphosphatidylinositol biosynthesis defect 15' SubClassOf 'central nervous system malformation' http://purl.obolibrary.org/obo/MONDO_0008071 autosomal dominant progressive nephropathy with hypertension 'autosomal dominant progressive nephropathy with hypertension' SubClassOf 'genetic hypertension' 'autosomal dominant progressive nephropathy with hypertension' SubClassOf 'kidney disease' http://purl.obolibrary.org/obo/MONDO_0011517 pseudohyperaldosteronism type 2 'pseudohyperaldosteronism type 2' SubClassOf 'hypertension, pregnancy-induced' 'pseudohyperaldosteronism type 2' SubClassOf 'genetic hypertension' 'pseudohyperaldosteronism type 2' SubClassOf 'bearer_of' some 'rare' 'pseudohyperaldosteronism type 2' SubClassOf 'pregnancy disorder' http://purl.obolibrary.org/obo/MONDO_0011577 myopathy, proximal, and ophthalmoplegia 'myopathy, proximal, and ophthalmoplegia' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0016059 cleft lip/palate-deafness-sacral lipoma syndrome 'cleft lip/palate-deafness-sacral lipoma syndrome' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0018582 GCGR-related hyperglucagonemia 'GCGR-related hyperglucagonemia' SubClassOf 'pancreatic neoplasm' 'GCGR-related hyperglucagonemia' SubClassOf 'pancreatic neoplasm' http://purl.obolibrary.org/obo/MONDO_0008913 cardiac valvular defect, developmental 'cardiac valvular defect, developmental' SubClassOf 'genetic cardiac anomaly' http://purl.obolibrary.org/obo/MONDO_0008965 CHARGE syndrome 'CHARGE syndrome' SubClassOf 'lens shape anomaly' http://www.ebi.ac.uk/efo/EFO_1000784 microscopic polyangiitis 'microscopic polyangiitis' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0008633 Muckle-Wells syndrome 'Muckle-Wells syndrome' SubClassOf 'secondary glomerular disease' 'Muckle-Wells syndrome' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0008641 retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 'retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations' SubClassOf 'disease of glomerular basement membrane' 'retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0008678 Williams syndrome 'Williams syndrome' SubClassOf 'neurovascular disorder' 'Williams syndrome' SubClassOf 'motor stereotypies' 'Williams syndrome' SubClassOf 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability' 'Williams syndrome' SubClassOf 'Mendelian neurodevelopmental disorder' 'Williams syndrome' SubClassOf 'congenital nervous system disorder' 'Williams syndrome' SubClassOf 'syndromic epicanthus' 'Williams syndrome' SubClassOf 'heart disease' 'Williams syndrome' SubClassOf 'partial deletion of the long arm of chromosome 7' 'Williams syndrome' SubClassOf 'genetic hypertension' 'Williams syndrome' SubClassOf 'Neurodevelopmental disorder' 'Williams syndrome' SubClassOf 'syndromic disease' 'Williams syndrome' SubClassOf 'partial deletion of the long arm of chromosome 7' http://purl.obolibrary.org/obo/MONDO_0018088 familial Mediterranean fever 'familial Mediterranean fever' SubClassOf 'secondary glomerular disease' 'familial Mediterranean fever' SubClassOf 'inherited kidney disorder' http://www.ebi.ac.uk/efo/EFO_0005297 Granulomatosis with Polyangiitis 'Granulomatosis with Polyangiitis' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0014306 vasculitis due to ADA2 deficiency 'vasculitis due to ADA2 deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100317 'vasculitis due to ADA2 deficiency' SubClassOf 'hereditary disorder of connective tissue' http://www.ebi.ac.uk/efo/EFO_0003063 polymyositis 'polymyositis' SubClassOf 'secondary glomerular disease' 'polymyositis' SubClassOf 'acquired idiopathic inflammatory myopathy' 'polymyositis' SubClassOf 'kidney disease' 'polymyositis' SubClassOf 'acquired idiopathic inflammatory myopathy' http://purl.obolibrary.org/obo/MONDO_0018965 Alport syndrome 'Alport syndrome' SubClassOf 'lens shape anomaly' http://purl.obolibrary.org/obo/MONDO_0018975 neurofibromatosis type 1 'neurofibromatosis type 1' SubClassOf 'eye disease' 'neurofibromatosis type 1' SubClassOf 'neurovascular disorder' 'neurofibromatosis type 1' SubClassOf 'genetic hypertension' http://purl.obolibrary.org/obo/MONDO_0100167 pulmonary disease, chronic obstructive, susceptibility to 'pulmonary disease, chronic obstructive, susceptibility to' SubClassOf 'predisposes towards' some 'chronic obstructive pulmonary disease' 'pulmonary disease, chronic obstructive, susceptibility to' SubClassOf 'inherited disease susceptibility' http://purl.obolibrary.org/obo/MONDO_0012203 familial hyperthyroidism due to mutations in TSH receptor 'familial hyperthyroidism due to mutations in TSH receptor' SubClassOf 'genetic hypertension' 'familial hyperthyroidism due to mutations in TSH receptor' SubClassOf 'bearer_of' some 'rare' http://www.ebi.ac.uk/efo/EFO_0007313 HIV-associated nephropathy 'HIV-associated nephropathy' SubClassOf 'focal segmental glomerulosclerosis' 'HIV-associated nephropathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0005363 http://www.ebi.ac.uk/efo/EFO_0007374 mixed connective tissue disease 'mixed connective tissue disease' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0014526 polyglucosan body myopathy type 2 'polyglucosan body myopathy type 2' SubClassOf 'disorder of glycogen metabolism' 'polyglucosan body myopathy type 2' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100314 http://purl.obolibrary.org/obo/MONDO_0007211 brachydactyly-arterial hypertension syndrome 'brachydactyly-arterial hypertension syndrome' SubClassOf 'genetic hypertension' http://purl.obolibrary.org/obo/MONDO_0009722 Bailey-Bloch congenital myopathy 'Bailey-Bloch congenital myopathy' SubClassOf 'congenital myopathy' 'Bailey-Bloch congenital myopathy' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0020121 muscular dystrophy 'muscular dystrophy' SubClassOf 'pulmonary disease, chronic obstructive, susceptibility to' http://purl.obolibrary.org/obo/MONDO_0019161 pseudohypoaldosteronism type 1 'pseudohypoaldosteronism type 1' SubClassOf 'pseudohypoaldosteronism' 'pseudohypoaldosteronism type 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100323 http://purl.obolibrary.org/obo/MONDO_0019162 pseudohypoaldosteronism type 2 'pseudohypoaldosteronism type 2' SubClassOf 'pseudohypoaldosteronism' 'pseudohypoaldosteronism type 2' SubClassOf 'genetic hypertension' 'pseudohypoaldosteronism type 2' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100323 http://www.ebi.ac.uk/efo/EFO_1001361 localised scleroderma 'localised scleroderma' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0009609 methylcobalamin deficiency type cblG 'methylcobalamin deficiency type cblG' SubClassOf 'inherited kidney disorder' 'methylcobalamin deficiency type cblG' SubClassOf 'thrombotic microangiopathy' 'methylcobalamin deficiency type cblG' SubClassOf 'inherited blood coagulation disorder' http://purl.obolibrary.org/obo/MONDO_0009671 intellectual disability-myopathy-short stature-endocrine defect syndrome 'intellectual disability-myopathy-short stature-endocrine defect syndrome' SubClassOf 'congenital myopathy' 'intellectual disability-myopathy-short stature-endocrine defect syndrome' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0007080 glucocorticoid-remediable aldosteronism 'glucocorticoid-remediable aldosteronism' SubClassOf 'genetic hypertension' http://purl.obolibrary.org/obo/MONDO_0007099 familial visceral amyloidosis 'familial visceral amyloidosis' SubClassOf 'secondary glomerular disease' 'familial visceral amyloidosis' SubClassOf 'inherited kidney disorder' 'familial visceral amyloidosis' SubClassOf 'bearer_of' some 'rare' http://www.ebi.ac.uk/efo/EFO_1001148 relapsing polychondritis 'relapsing polychondritis' SubClassOf 'secondary glomerular disease' http://www.ebi.ac.uk/efo/EFO_1001209 temporal arteritis 'temporal arteritis' SubClassOf 'secondary glomerular disease' 'temporal arteritis' SubClassOf 'kidney disease' http://www.ebi.ac.uk/efo/EFO_1001211 thromboangiitis obliterans 'thromboangiitis obliterans' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0000959 malignant hypertensive renal disease 'malignant hypertensive renal disease' SubClassOf 'genetic hypertension' http://www.ebi.ac.uk/efo/EFO_1001186 Sneddon syndrome 'Sneddon syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100317 'Sneddon syndrome' SubClassOf 'genetic skin disorder' http://purl.obolibrary.org/obo/MONDO_0012833 Crouzon syndrome-acanthosis nigricans syndrome 'Crouzon syndrome-acanthosis nigricans syndrome' SubClassOf 'focal segmental glomerulosclerosis' http://purl.obolibrary.org/obo/MONDO_0010122 congenital thrombotic thrombocytopenic purpura 'congenital thrombotic thrombocytopenic purpura' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0007915 systemic lupus erythematosus 'systemic lupus erythematosus' SubClassOf 'thrombotic microangiopathy' 'systemic lupus erythematosus' SubClassOf 'secondary glomerular disease' 'systemic lupus erythematosus' SubClassOf 'kidney disease' http://purl.obolibrary.org/obo/MONDO_0032936 myopathy, congenital, with respiratory insufficiency and bone fractures 'myopathy, congenital, with respiratory insufficiency and bone fractures' SubClassOf 'genetic disorder' 'myopathy, congenital, with respiratory insufficiency and bone fractures' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0032937 myopathy, congenital proximal, with minicore lesions 'myopathy, congenital proximal, with minicore lesions' SubClassOf 'genetic disorder' 'myopathy, congenital proximal, with minicore lesions' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0019952 congenital myopathy 'congenital myopathy' SubClassOf 'pulmonary disease, chronic obstructive, susceptibility to' http://purl.obolibrary.org/obo/UBERON_0011143 upper urinary tract 'upper urinary tract' SubClassOf 'anatomical entity' 'upper urinary tract' SubClassOf 'part of' some 'anatomical system' 'upper urinary tract' SubClassOf 'anatomical structure' http://purl.obolibrary.org/obo/MONDO_0019724 secondary glomerular disease 'secondary glomerular disease' SubClassOf 'glomerular disease' http://purl.obolibrary.org/obo/MONDO_0019737 thrombotic microangiopathy 'thrombotic microangiopathy' SubClassOf 'kidney disease' http://purl.obolibrary.org/obo/MONDO_0007788 hypertriglyceridemia, familial 'hypertriglyceridemia, familial' SubClassOf 'major hypertriglyceridemia' 'hypertriglyceridemia, familial' SubClassOf 'familial hyperlipidemia' 'hypertriglyceridemia, familial' EquivalentTo 'Hypertriglyceridemia' and ('bearer_of' some 'inherited') 'hypertriglyceridemia, familial' SubClassOf 'Hypertriglyceridemia' http://purl.obolibrary.org/obo/MONDO_0007781 essential hypertension, genetic 'essential hypertension, genetic' SubClassOf 'genetic hypertension' 'essential hypertension, genetic' SubClassOf 'genetic disorder' http://purl.obolibrary.org/obo/MONDO_0044746 zoonotic bacterial infection 'zoonotic bacterial infection' SubClassOf 'bacterial disease' 'zoonotic bacterial infection' SubClassOf 'zoonosis' http://purl.obolibrary.org/obo/MONDO_0017148 heritable pulmonary arterial hypertension 'heritable pulmonary arterial hypertension' SubClassOf 'genetic hypertension' 'heritable pulmonary arterial hypertension' SubClassOf 'genetic disorder' http://purl.obolibrary.org/obo/MONDO_0019439 AA amyloidosis 'AA amyloidosis' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0019438 AL amyloidosis 'AL amyloidosis' SubClassOf 'secondary glomerular disease' http://purl.obolibrary.org/obo/MONDO_0009925 autosomal recessive inherited pseudoxanthoma elasticum 'autosomal recessive inherited pseudoxanthoma elasticum' SubClassOf 'genetic hypertension' 'autosomal recessive inherited pseudoxanthoma elasticum' SubClassOf 'familial restrictive cardiomyopathy' 'autosomal recessive inherited pseudoxanthoma elasticum' SubClassOf 'developmental defect during embryogenesis' 'autosomal recessive inherited pseudoxanthoma elasticum' SubClassOf 'eye disease' 'autosomal recessive inherited pseudoxanthoma elasticum' SubClassOf 'bearer_of' some 'rare' http://purl.obolibrary.org/obo/MONDO_0010977 Brody myopathy 'Brody myopathy' SubClassOf 'myopathy' 'Brody myopathy' SubClassOf 'qualitative or quantitative defects of protein SERCA1' 'Brody myopathy' SubClassOf 'myopathy' 'Brody myopathy' SubClassOf 'qualitative or quantitative defects of protein SERCA1' http://purl.obolibrary.org/obo/MONDO_0019391 Fanconi anemia 'Fanconi anemia' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0015512 genetic hypertension 'genetic hypertension' SubClassOf 'bearer_of' some 'rare' 'genetic hypertension' EquivalentTo 'hypertension' and ('bearer_of' some 'inherited') 'genetic hypertension' SubClassOf 'inherited kidney disorder' 'genetic hypertension' SubClassOf 'hypertension' 'genetic hypertension' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0017984 familial lambdoid synostosis 'familial lambdoid synostosis' SubClassOf 'isolated craniosynostosis' 'familial lambdoid synostosis' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0030701 autoimmune cardiomyopathy 'autoimmune cardiomyopathy' SubClassOf 'cardiomyopathy' 'autoimmune cardiomyopathy' SubClassOf 'autoimmune disorder of musculoskeletal system' 'autoimmune cardiomyopathy' SubClassOf 'autoimmune disorder of cardiovascular system' http://www.ebi.ac.uk/efo/EFO_0004236 focal segmental glomerulosclerosis 'focal segmental glomerulosclerosis' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0011309 familial gestational hyperthyroidism 'familial gestational hyperthyroidism' SubClassOf 'hypertension, pregnancy-induced' 'familial gestational hyperthyroidism' SubClassOf 'genetic hypertension' 'familial gestational hyperthyroidism' SubClassOf 'bearer_of' some 'rare' 'familial gestational hyperthyroidism' SubClassOf 'pregnancy disorder' http://purl.obolibrary.org/obo/MONDO_0011303 focal segmental glomerulosclerosis 1 'focal segmental glomerulosclerosis 1' SubClassOf 'focal segmental glomerulosclerosis' 'focal segmental glomerulosclerosis 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0005363 http://purl.obolibrary.org/obo/MONDO_0011382 sickle cell anemia 'sickle cell anemia' SubClassOf 'inherited kidney disorder' 'sickle cell anemia' SubClassOf 'secondary avascular necrosis' 'sickle cell anemia' SubClassOf 'congenital hypogonadotropic hypogonadism' 'sickle cell anemia' SubClassOf 'avascular necrosis of genetic origin' http://purl.obolibrary.org/obo/MONDO_0011399 alpha thalassemia 'alpha thalassemia' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0013731 MEGF10-Related Myopathy 'MEGF10-Related Myopathy' SubClassOf 'congenital myopathy' 'MEGF10-Related Myopathy' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0013743 autosomal systemic lupus erythematosus type 16 'autosomal systemic lupus erythematosus type 16' SubClassOf 'inherited blood coagulation disorder' http://purl.obolibrary.org/obo/MONDO_0025481 zoonosis 'zoonosis' SubClassOf 'infectious disease' http://purl.obolibrary.org/obo/MONDO_0001549 hemolytic-uremic syndrome 'hemolytic-uremic syndrome' SubClassOf 'inherited kidney disorder' http://purl.obolibrary.org/obo/MONDO_0013458 hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome 'hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome' SubClassOf 'genetic hypertension' http://purl.obolibrary.org/obo/MONDO_0013276 Reynolds syndrome 'Reynolds syndrome' SubClassOf 'secondary glomerular disease' 'Reynolds syndrome' SubClassOf 'type II hypersensitivity reaction disease' http://purl.obolibrary.org/obo/MONDO_0013291 glycogen storage disease XV 'glycogen storage disease XV' SubClassOf 'disorder of glycogen metabolism' 'glycogen storage disease XV' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100314 http://purl.obolibrary.org/obo/UBERON_0003153 head capsule 'head capsule' SubClassOf 'anatomical entity' 'head capsule' SubClassOf 'part of' some 'integumental system' 'head capsule' SubClassOf 'part of' some 'anatomical system' 'head capsule' SubClassOf 'anatomical structure' http://purl.obolibrary.org/obo/MONDO_0025303 anaplasmosis 'anaplasmosis' SubClassOf 'zoonotic bacterial infection' http://www.ebi.ac.uk/efo/EFO_0700016 Smart-seq v4 'Smart-seq v4' SubClassOf 'Smart-like' 'Smart-seq v4' SubClassOf 'assay' http://purl.obolibrary.org/obo/MONDO_0100314 GYG1-related disorder of glycogen metabolism 'GYG1-related disorder of glycogen metabolism' SubClassOf 'disorder of glycogen metabolism' http://purl.obolibrary.org/obo/MONDO_0100317 deficiency of adenosine deaminase 2 'deficiency of adenosine deaminase 2' SubClassOf 'genetic disorder' http://purl.obolibrary.org/obo/MONDO_0100323 inherited pseudohypoaldosteronism 'inherited pseudohypoaldosteronism' SubClassOf 'pseudohypoaldosteronism' 'inherited pseudohypoaldosteronism' SubClassOf 'inherited kidney disorder' 'inherited pseudohypoaldosteronism' EquivalentTo 'pseudohypoaldosteronism' and ('bearer_of' some 'inherited') http://purl.obolibrary.org/obo/HP_0030158 Cervical ectropion 'Cervical ectropion' SubClassOf 'Abnormality of the uterus' http://www.ebi.ac.uk/efo/EFO_0803376 erythrocyte deformability 'erythrocyte deformability' SubClassOf 'hemorheological measurement' http://www.ebi.ac.uk/efo/EFO_0803377 metachronous colorectal adenoma 'metachronous colorectal adenoma' SubClassOf 'colorectal adenoma' http://www.ebi.ac.uk/efo/EFO_0803378 visual masking mesurement 'visual masking mesurement' SubClassOf 'visual perception measurement' http://www.ebi.ac.uk/efo/EFO_0803379 anti-GAD65 autoimmune neurological syndromes 'anti-GAD65 autoimmune neurological syndromes' SubClassOf 'autoimmune disease' http://www.ebi.ac.uk/efo/EFO_0803380 cardiovascular age measurement 'cardiovascular age measurement' SubClassOf 'cardiovascular measurement' http://www.ebi.ac.uk/efo/EFO_0803381 fornix volume measurement 'fornix volume measurement' SubClassOf 'hippocampal volume' http://www.ebi.ac.uk/efo/EFO_0803369 vascular endothelial function measurement 'vascular endothelial function measurement' SubClassOf 'cardiovascular measurement' http://www.ebi.ac.uk/efo/EFO_0803370 photoreceptor cell layer thickness measurement 'photoreceptor cell layer thickness measurement' SubClassOf 'retinal layer thickness measurement' http://www.ebi.ac.uk/efo/EFO_0803371 outer nuclear layer thickness measurement 'outer nuclear layer thickness measurement' SubClassOf 'photoreceptor cell layer thickness measurement' http://www.ebi.ac.uk/efo/EFO_0803372 inner segment thickness measurement 'inner segment thickness measurement' SubClassOf 'photoreceptor cell layer thickness measurement' http://www.ebi.ac.uk/efo/EFO_0803373 outer segment thickness measurement 'outer segment thickness measurement' SubClassOf 'photoreceptor cell layer thickness measurement' http://www.ebi.ac.uk/efo/EFO_0803374 hemorheological measurement 'hemorheological measurement' SubClassOf 'hematological measurement' http://www.ebi.ac.uk/efo/EFO_0803375 erythrocyte aggregation 'erythrocyte aggregation' SubClassOf 'hemorheological measurement' http://purl.obolibrary.org/obo/MONDO_0005363 inherited focal segmental glomerulosclerosis 'inherited focal segmental glomerulosclerosis' SubClassOf 'inherited kidney disorder' 'inherited focal segmental glomerulosclerosis' EquivalentTo 'focal segmental glomerulosclerosis' and ('bearer_of' some 'inherited') 'inherited focal segmental glomerulosclerosis' SubClassOf 'focal segmental glomerulosclerosis' http://purl.obolibrary.org/obo/MONDO_0100167 pulmonary disease, chronic obstructive, susceptibility to 'pulmonary disease, chronic obstructive, susceptibility to' SubClassOf 'predisposes towards' some 'chronic obstructive pulmonary disease' 'pulmonary disease, chronic obstructive, susceptibility to' SubClassOf 'inherited disease susceptibility' http://purl.obolibrary.org/obo/MONDO_0019724 secondary glomerular disease 'secondary glomerular disease' SubClassOf 'glomerular disease' http://purl.obolibrary.org/obo/MONDO_0007788 hypertriglyceridemia, familial 'hypertriglyceridemia, familial' SubClassOf 'major hypertriglyceridemia' 'hypertriglyceridemia, familial' SubClassOf 'familial hyperlipidemia' 'hypertriglyceridemia, familial' EquivalentTo 'Hypertriglyceridemia' and ('bearer_of' some 'inherited') 'hypertriglyceridemia, familial' SubClassOf 'Hypertriglyceridemia' http://purl.obolibrary.org/obo/MONDO_0044746 zoonotic bacterial infection 'zoonotic bacterial infection' SubClassOf 'bacterial disease' 'zoonotic bacterial infection' SubClassOf 'zoonosis' http://purl.obolibrary.org/obo/MONDO_0030701 autoimmune cardiomyopathy 'autoimmune cardiomyopathy' SubClassOf 'cardiomyopathy' 'autoimmune cardiomyopathy' SubClassOf 'autoimmune disorder of musculoskeletal system' 'autoimmune cardiomyopathy' SubClassOf 'autoimmune disorder of cardiovascular system' http://purl.obolibrary.org/obo/MONDO_0025481 zoonosis 'zoonosis' SubClassOf 'infectious disease'