88 20 5 http://www.orpha.net/ORDO/Orphanet_397750 Periodic paralysis with later-onset distal motor neuropathy 'Periodic paralysis with later-onset distal motor neuropathy' SubClassOf 'congenital nervous system disorder' http://www.orpha.net/ORDO/Orphanet_397755 Periodic paralysis with transient compartment-like syndrome 'Periodic paralysis with transient compartment-like syndrome' SubClassOf 'Genetic peripheral neuropathy' http://www.orpha.net/ORDO/Orphanet_324604 Classic multiminicore myopathy 'Classic multiminicore myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100175 http://www.ebi.ac.uk/efo/EFO_0000516 glaucoma 'glaucoma' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_1423 Lethal recessive chondrodysplasia 'Lethal recessive chondrodysplasia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0022723 http://purl.obolibrary.org/obo/MONDO_0023616 familial leiomyomatosis 'familial leiomyomatosis' EquivalentTo 'leiomyomatosis' and ('has modifier' some 'inherited') 'familial leiomyomatosis' SubClassOf 'Genetic soft tissue tumor' 'familial leiomyomatosis' SubClassOf 'leiomyomatosis' http://www.orpha.net/ORDO/Orphanet_1155 Arthrogryposis due to muscular dystrophy 'Arthrogryposis due to muscular dystrophy' SubClassOf 'congenital nervous system disorder' http://www.orpha.net/ORDO/Orphanet_169186 Autosomal recessive centronuclear myopathy 'Autosomal recessive centronuclear myopathy' SubClassOf 'Qualitative or quantitative defects of titin' 'Autosomal recessive centronuclear myopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100175 http://purl.obolibrary.org/obo/MONDO_0016105 acquired skeletal muscle disease 'acquired skeletal muscle disease' SubClassOf 'acquired peripheral neuropathy' 'acquired skeletal muscle disease' SubClassOf 'has modifier' some 'acquired' http://purl.obolibrary.org/obo/MONDO_0016125 infectious, fungal or parasitic myopathy 'infectious, fungal or parasitic myopathy' SubClassOf 'infectious disease of the nervous system' 'infectious, fungal or parasitic myopathy' SubClassOf 'infectious disease' http://www.orpha.net/ORDO/Orphanet_206634 Genetic skeletal muscle disease 'Genetic skeletal muscle disease' SubClassOf 'neuromuscular disease' 'Genetic skeletal muscle disease' SubClassOf 'Genetic peripheral neuropathy' http://www.ebi.ac.uk/efo/EFO_0002179 G401 'G401' SubClassOf 'cancer cell line' http://www.ebi.ac.uk/efo/EFO_0002034 G1E 'G1E' SubClassOf 'derives_from' some 'embryo' http://www.ebi.ac.uk/efo/EFO_0002055 G1E-ER4 'G1E-ER4' SubClassOf 'derives_from' some 'embryo' http://www.ebi.ac.uk/efo/EFO_0002074 PC-3 'PC-3' SubClassOf 'cancer cell line' http://www.ebi.ac.uk/efo/EFO_1000850 burning mouth syndrome 'burning mouth syndrome' SubClassOf 'headache disorder' http://www.ebi.ac.uk/efo/EFO_1000906 dry eye syndrome 'dry eye syndrome' SubClassOf 'has_disease_location' some ('conjunctiva' or ('part of' some 'conjunctiva')) http://www.ebi.ac.uk/efo/EFO_1000918 endolymphatic hydrops 'endolymphatic hydrops' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_363409 Fetal akinesia-cerebral and retinal hemorrhage syndrome 'Fetal akinesia-cerebral and retinal hemorrhage syndrome' SubClassOf 'congenital nervous system disorder' http://www.orpha.net/ORDO/Orphanet_206707 Bulbospinal muscular atrophy of adult 'Bulbospinal muscular atrophy of adult' SubClassOf 'Proximal spinal muscular atrophy type 4' http://www.orpha.net/ORDO/Orphanet_206704 Bulbospinal muscular atrophy of children 'Bulbospinal muscular atrophy of children' SubClassOf 'Proximal spinal muscular atrophy type 3' http://www.ebi.ac.uk/efo/EFO_0002625 teratozoospermia 'teratozoospermia' SubClassOf 'male reproductive system disease' 'teratozoospermia' EquivalentTo 'realized_in' some ('disease course' and ('has_quality' some 'abnormal') and ('has_disease_location' some 'sperm')) 'teratozoospermia' SubClassOf 'has_disease_location' some 'male reproductive system' 'teratozoospermia' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.orpha.net/ORDO/Orphanet_289377 Early-onset myopathy with fatal cardiomyopathy 'Early-onset myopathy with fatal cardiomyopathy' SubClassOf 'Non-dystrophic myopathy' 'Early-onset myopathy with fatal cardiomyopathy' SubClassOf 'Qualitative or quantitative defects of titin' 'Early-onset myopathy with fatal cardiomyopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100175 http://www.ebi.ac.uk/efo/EFO_0002509 progressive external ophthalmoplegia 'progressive external ophthalmoplegia' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_43115 Hereditary myopathy with lactic acidosis due to ISCU deficiency 'Hereditary myopathy with lactic acidosis due to ISCU deficiency' SubClassOf 'congenital nervous system disorder' http://www.orpha.net/ORDO/Orphanet_79102 Thyrotoxic periodic paralysis 'Thyrotoxic periodic paralysis' SubClassOf 'Genetic peripheral neuropathy' http://www.ebi.ac.uk/efo/EFO_0005269 congenital heart malformation 'congenital heart malformation' SubClassOf 'disorder of development or morphogenesis' http://www.orpha.net/ORDO/Orphanet_90673 Hypothyroidism due to TSH receptor mutations 'Hypothyroidism due to TSH receptor mutations' SubClassOf 'disease of signal transduction' http://www.ebi.ac.uk/efo/EFO_0005187 C-peptide measurement 'C-peptide measurement' SubClassOf 'insulin secretion measurement' http://www.ebi.ac.uk/efo/EFO_0005441 DU 145 'DU 145' SubClassOf 'derives_from' some 'prostate gland' http://www.orpha.net/ORDO/Orphanet_99104 Atrial septal defect, coronary sinus type 'Atrial septal defect, coronary sinus type' SubClassOf 'syndromic disease' http://www.ebi.ac.uk/efo/EFO_0003063 polymyositis 'polymyositis' SubClassOf 'Genetic peripheral neuropathy' 'polymyositis' SubClassOf 'acquired peripheral neuropathy' http://www.orpha.net/ORDO/Orphanet_217052 Early-onset non-syndromic cataract 'Early-onset non-syndromic cataract' SubClassOf 'Rare genetic neurological disorder' http://www.orpha.net/ORDO/Orphanet_97229 Riboflavin transporter deficiency 'Riboflavin transporter deficiency' SubClassOf 'Syndromic genetic deafness' 'Riboflavin transporter deficiency' SubClassOf 'Bulbospinal muscular atrophy of children' 'Riboflavin transporter deficiency' SubClassOf 'Syndromic genetic deafness' 'Riboflavin transporter deficiency' SubClassOf 'motor neuron disease' 'Riboflavin transporter deficiency' SubClassOf 'disease has major feature' some 'Bulbospinal muscular atrophy' 'Riboflavin transporter deficiency' SubClassOf 'Bulbospinal muscular atrophy of children' http://www.ebi.ac.uk/efo/EFO_0009543 disturbances of sensation of smell and taste 'disturbances of sensation of smell and taste' SubClassOf 'sensory system disease' 'disturbances of sensation of smell and taste' SubClassOf 'Abnormality of the sense of smell' 'disturbances of sensation of smell and taste' SubClassOf 'Abnormality of taste sensation' http://www.ebi.ac.uk/efo/EFO_0007216 congenital diaphragmatic hernia 'congenital diaphragmatic hernia' SubClassOf 'diaphragmatic hernia' 'congenital diaphragmatic hernia' SubClassOf 'congenital nervous system disorder' 'congenital diaphragmatic hernia' SubClassOf 'disease has feature' some 'diaphragmatic hernia' http://www.ebi.ac.uk/efo/EFO_0007299 hemorrhagic fever with renal syndrome 'hemorrhagic fever with renal syndrome' SubClassOf 'viral hemorrhagic fever' http://www.orpha.net/ORDO/Orphanet_319332 Autosomal recessive myogenic arthrogryposis multiplex congenita 'Autosomal recessive myogenic arthrogryposis multiplex congenita' SubClassOf 'congenital nervous system disorder' http://purl.obolibrary.org/obo/MONDO_0002847 skeletal muscle cancer 'skeletal muscle cancer' SubClassOf 'peripheral nervous system cancer' http://purl.obolibrary.org/obo/MONDO_0002848 skeletal muscle neoplasm 'skeletal muscle neoplasm' SubClassOf 'peripheral nervous system neoplasm' 'skeletal muscle neoplasm' SubClassOf 'neoplasm' http://purl.obolibrary.org/obo/MONDO_0024239 congenital anomaly of cardiovascular system 'congenital anomaly of cardiovascular system' SubClassOf 'disorder of development or morphogenesis' http://www.ebi.ac.uk/efo/EFO_0007420 paratyphoid fever 'paratyphoid fever' SubClassOf 'primary bacterial infectious disease' 'paratyphoid fever' SubClassOf 'rare form of salmonellosis' 'paratyphoid fever' SubClassOf 'salmonellosis' http://purl.obolibrary.org/obo/MONDO_0014689 Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome 'Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome' SubClassOf 'congenital nervous system disorder' http://www.ebi.ac.uk/efo/EFO_0005023 adipose tissue derived mesenchymal stem cell 'adipose tissue derived mesenchymal stem cell' SubClassOf 'derives_from' some 'adipose tissue' http://www.orpha.net/ORDO/Orphanet_163665 Spondyloepiphyseal dysplasia tarda, Kohn type 'Spondyloepiphyseal dysplasia tarda, Kohn type' SubClassOf 'Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia' 'Spondyloepiphyseal dysplasia tarda, Kohn type' SubClassOf 'Spondyloepiphyseal dysplasia tarda' http://www.orpha.net/ORDO/Orphanet_83420 Proximal spinal muscular atrophy type 4 'Proximal spinal muscular atrophy type 4' SubClassOf 'Werdnig-Hoffmann disease' 'Proximal spinal muscular atrophy type 4' SubClassOf 'Proximal spinal muscular atrophy' http://www.orpha.net/ORDO/Orphanet_83419 Proximal spinal muscular atrophy type 3 'Proximal spinal muscular atrophy type 3' SubClassOf 'Werdnig-Hoffmann disease' 'Proximal spinal muscular atrophy type 3' SubClassOf 'Proximal spinal muscular atrophy' http://www.orpha.net/ORDO/Orphanet_83418 Proximal spinal muscular atrophy type 2 'Proximal spinal muscular atrophy type 2' SubClassOf 'Werdnig-Hoffmann disease' 'Proximal spinal muscular atrophy type 2' SubClassOf 'Proximal spinal muscular atrophy' http://www.orpha.net/ORDO/Orphanet_2674 Cyprus facial-neuromusculoskeletal syndrome 'Cyprus facial-neuromusculoskeletal syndrome' SubClassOf 'congenital nervous system disorder' http://www.ebi.ac.uk/efo/EFO_0001639 cancer cell line 'cancer cell line' SubClassOf 'derives_from' some 'cancer' http://www.orpha.net/ORDO/Orphanet_2596 Myopathy and diabetes mellitus 'Myopathy and diabetes mellitus' SubClassOf 'congenital nervous system disorder' http://www.orpha.net/ORDO/Orphanet_2591 Infantile myofibromatosis 'Infantile myofibromatosis' SubClassOf 'benign neoplasm of peripheral nervous system' http://purl.obolibrary.org/obo/MONDO_0020122 idiopathic inflammatory myopathy 'idiopathic inflammatory myopathy' SubClassOf 'autoimmune neuropathy' http://purl.obolibrary.org/obo/MONDO_0009669 Werdnig-Hoffmann disease 'Werdnig-Hoffmann disease' SubClassOf 'Proximal spinal muscular atrophy' http://purl.obolibrary.org/obo/MONDO_0044014 postpartum thyroiditis 'postpartum thyroiditis' SubClassOf 'puerperal disorder' 'postpartum thyroiditis' SubClassOf 'autoimmune thyroid disease' 'postpartum thyroiditis' EquivalentTo 'thyroiditis (disease)' and 'puerperal disorder' http://www.ebi.ac.uk/efo/EFO_1001409 Pyomyositis 'Pyomyositis' SubClassOf 'has modifier' some 'rare' http://www.ebi.ac.uk/efo/EFO_1001403 Postpartum Thyroiditis 'Postpartum Thyroiditis' EquivalentTo 'thyroiditis (disease)' and 'puerperal disorder' 'Postpartum Thyroiditis' SubClassOf 'autoimmune thyroid disease' 'Postpartum Thyroiditis' SubClassOf 'puerperal disorder' http://www.ebi.ac.uk/efo/EFO_1001049 mucoepidermoid tumor 'mucoepidermoid tumor' SubClassOf 'adenocarcinoma' 'mucoepidermoid tumor' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.ebi.ac.uk/efo/EFO_1001155 retinal drusen 'retinal drusen' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_178464 Hereditary proximal myopathy with early respiratory failure 'Hereditary proximal myopathy with early respiratory failure' SubClassOf 'Qualitative or quantitative defects of titin' 'Hereditary proximal myopathy with early respiratory failure' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100175 http://www.ebi.ac.uk/efo/EFO_1001176 sensorineural hearing loss 'sensorineural hearing loss' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_139 CHILD syndrome 'CHILD syndrome' SubClassOf 'Rare genetic neurological disorder' http://www.ebi.ac.uk/efo/EFO_1001001 keratoconjunctivitis sicca 'keratoconjunctivitis sicca' SubClassOf 'eye disease' 'keratoconjunctivitis sicca' SubClassOf 'has_disease_location' some ('conjunctiva' or ('part of' some 'conjunctiva')) 'keratoconjunctivitis sicca' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.orpha.net/ORDO/Orphanet_359 Hereditary glaucoma 'Hereditary glaucoma' SubClassOf 'Rare genetic neurological disorder' http://www.orpha.net/ORDO/Orphanet_614 Thomsen and Becker disease 'Thomsen and Becker disease' SubClassOf 'Genetic peripheral neuropathy' http://www.orpha.net/ORDO/Orphanet_684 Paramyotonia congenita of Von Eulenburg 'Paramyotonia congenita of Von Eulenburg' SubClassOf 'Genetic peripheral neuropathy' http://www.ebi.ac.uk/efo/EFO_0001059 cataract 'cataract' SubClassOf 'sensory system disease' http://www.orpha.net/ORDO/Orphanet_612 Potassium-aggravated myotonia 'Potassium-aggravated myotonia' SubClassOf 'Genetic peripheral neuropathy' http://www.orpha.net/ORDO/Orphanet_523 Hereditary leiomyomatosis and renal cell cancer 'Hereditary leiomyomatosis and renal cell cancer' SubClassOf 'kidney neoplasm' 'Hereditary leiomyomatosis and renal cell cancer' SubClassOf 'Genetic soft tissue tumor' 'Hereditary leiomyomatosis and renal cell cancer' SubClassOf 'renal leiomyoma' 'Hereditary leiomyomatosis and renal cell cancer' SubClassOf http://purl.obolibrary.org/obo/MONDO_0003291 'Hereditary leiomyomatosis and renal cell cancer' SubClassOf 'leiomyomatosis' http://www.ebi.ac.uk/efo/EFO_0003971 MEL cell line 'MEL cell line' SubClassOf 'cancer cell line' http://www.ebi.ac.uk/efo/EFO_0001253 THP-1 'THP-1' SubClassOf 'derives_from' some 'blood' http://www.ebi.ac.uk/efo/EFO_0003845 kidney stone 'kidney stone' SubClassOf 'nephrolithiasis' 'kidney stone' SubClassOf http://www.w3.org/2002/07/owl#Thing http://www.orpha.net/ORDO/Orphanet_754 Androgen insensitivity syndrome 'Androgen insensitivity syndrome' SubClassOf 'disease of signal transduction' http://www.ebi.ac.uk/efo/EFO_1001758 ageusia 'ageusia' SubClassOf 'sensory system disease' 'ageusia' SubClassOf 'Abnormality of taste sensation' http://www.ebi.ac.uk/efo/EFO_1001866 ventral hernia 'ventral hernia' SubClassOf 'disease' 'ventral hernia' SubClassOf 'has_disease_location' some ('abdominal wall' or ('part of' some 'abdominal wall')) http://purl.obolibrary.org/obo/MONDO_0019331 rare form of salmonellosis 'rare form of salmonellosis' SubClassOf 'has modifier' some 'rare' 'rare form of salmonellosis' SubClassOf 'bacterial disease' http://www.ebi.ac.uk/efo/EFO_0001365 age-related macular degeneration 'age-related macular degeneration' SubClassOf 'sensory system disease' http://www.ebi.ac.uk/efo/EFO_0006789 typhoid fever 'typhoid fever' SubClassOf 'salmonellosis' 'typhoid fever' SubClassOf 'rare form of salmonellosis' 'typhoid fever' SubClassOf 'salmonellosis' http://www.ebi.ac.uk/efo/EFO_0004389 UCH-1 'UCH-1' SubClassOf 'cancer cell line' http://www.ebi.ac.uk/efo/EFO_0004248 male infertility 'male infertility' SubClassOf 'teratozoospermia' http://www.orpha.net/ORDO/Orphanet_37553 Cardiodysrhythmic potassium-sensitive periodic paralysis 'Cardiodysrhythmic potassium-sensitive periodic paralysis' SubClassOf 'Genetic peripheral neuropathy' http://www.ebi.ac.uk/efo/EFO_0008561 diaphragmatic hernia 'diaphragmatic hernia' SubClassOf 'diaphragm disease' http://www.orpha.net/ORDO/Orphanet_98641 Syndromic cataract 'Syndromic cataract' SubClassOf 'Rare genetic neurological disorder' http://www.orpha.net/ORDO/Orphanet_98645 Cerebral disease with cataract 'Cerebral disease with cataract' SubClassOf 'Rare genetic neurological disorder' http://purl.obolibrary.org/obo/MONDO_0001589 vaginal enterocele 'vaginal enterocele' SubClassOf 'vaginal disease' 'vaginal enterocele' SubClassOf 'small intestine disease' 'vaginal enterocele' SubClassOf 'prolapse of female genital organ' 'vaginal enterocele' SubClassOf 'connective tissue disease' 'vaginal enterocele' SubClassOf http://www.w3.org/2002/07/owl#Thing http://purl.obolibrary.org/obo/MONDO_0001592 prolapse of female genital organ 'prolapse of female genital organ' SubClassOf 'female reproductive system disease' http://purl.obolibrary.org/obo/MONDO_0025445 Wieacker-Wolff syndrome (spectrum) 'Wieacker-Wolff syndrome (spectrum)' SubClassOf 'congenital nervous system disorder' http://purl.obolibrary.org/obo/MONDO_0001328 thyroid hormone resistance syndrome 'thyroid hormone resistance syndrome' SubClassOf 'disease of signal transduction' http://purl.obolibrary.org/obo/MONDO_0021115 luminal B breast carcinoma 'luminal B breast carcinoma' SubClassOf 'breast tumor luminal' http://purl.obolibrary.org/obo/MONDO_0021116 luminal A breast carcinoma 'luminal A breast carcinoma' SubClassOf 'breast tumor luminal' http://purl.obolibrary.org/obo/MONDO_0018661 Zika virus infectious disease 'Zika virus infectious disease' SubClassOf 'Flaviviridae infectious disease' 'Zika virus infectious disease' SubClassOf 'disease has feature' some 'conjunctivitis' 'Zika virus infectious disease' SubClassOf 'vector-borne disease' 'Zika virus infectious disease' SubClassOf 'has modifier' some 'rare' http://purl.obolibrary.org/obo/MONDO_0004651 smallpox 'smallpox' SubClassOf 'viral disease' http://purl.obolibrary.org/obo/MONDO_0100175 TTN-related myopathy 'TTN-related myopathy' SubClassOf 'Qualitative or quantitative defects of titin' 'TTN-related myopathy' SubClassOf 'Congenital myopathy' http://purl.obolibrary.org/obo/CHEBI_135752 tafenoquine 'tafenoquine' SubClassOf 'chemical entity' http://www.ebi.ac.uk/efo/EFO_0010815 remnant cholesterol measurement 'remnant cholesterol measurement' SubClassOf 'lipoprotein measurement' http://www.ebi.ac.uk/efo/EFO_0010813 fasting C-peptide measurement 'fasting C-peptide measurement' SubClassOf 'C-peptide measurement' http://www.ebi.ac.uk/efo/EFO_0010814 proinsulin measurement 'proinsulin measurement' SubClassOf 'insulin measurement' http://www.ebi.ac.uk/efo/EFO_0010811 carbohydrate intake measurement 'carbohydrate intake measurement' SubClassOf 'diet measurement' http://www.ebi.ac.uk/efo/EFO_0010812 T-cell immunoglobulin and mucin domain 1 measurement 'T-cell immunoglobulin and mucin domain 1 measurement' SubClassOf 'protein measurement' http://www.ebi.ac.uk/efo/EFO_0010810 protein intake measurement 'protein intake measurement' SubClassOf 'diet measurement' http://www.ebi.ac.uk/efo/EFO_0010808 response to tafenoquine 'response to tafenoquine' SubClassOf 'response to drug' 'response to tafenoquine' SubClassOf 'is_about' some 'tafenoquine' http://www.ebi.ac.uk/efo/EFO_0010809 fat intake measurement 'fat intake measurement' SubClassOf 'diet measurement' http://www.ebi.ac.uk/efo/EFO_0010806 enrichment of phosphorylated protein 'enrichment of phosphorylated protein' SubClassOf 'enrichment process' http://www.ebi.ac.uk/efo/EFO_0010807 F121-9 'F121-9' SubClassOf 'ES cell line' 'F121-9' SubClassOf 'has_quality' some 'female' 'F121-9' SubClassOf 'part of' some 'blastocyst' http://www.ebi.ac.uk/efo/EFO_0010805 massively parallel signature sequencing 'massively parallel signature sequencing' SubClassOf 'DNA-seq' http://purl.obolibrary.org/obo/MONDO_0022723 chondrodysplasia 'chondrodysplasia' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0000890 Zika virus congenital syndrome 'Zika virus congenital syndrome' SubClassOf 'congenital abnormality' 'Zika virus congenital syndrome' SubClassOf 'post-viral disorder' 'Zika virus congenital syndrome' SubClassOf 'disease arises from feature' some 'Zika virus infectious disease' 'Zika virus congenital syndrome' SubClassOf 'post-infectious syndrome' 'Zika virus congenital syndrome' EquivalentTo 'congenital abnormality' and ('disease arises from feature' some 'Zika virus infectious disease') http://purl.obolibrary.org/obo/MONDO_0003291 leiomyoma cutis 'leiomyoma cutis' SubClassOf 'benign neoplasm of skin' 'leiomyoma cutis' SubClassOf 'leiomyoma' 'leiomyoma cutis' SubClassOf 'dermis tumor' http://purl.obolibrary.org/obo/MONDO_0023616 familial leiomyomatosis 'familial leiomyomatosis' EquivalentTo 'leiomyomatosis' and ('has modifier' some 'inherited') 'familial leiomyomatosis' SubClassOf 'Genetic soft tissue tumor' 'familial leiomyomatosis' SubClassOf 'leiomyomatosis' http://purl.obolibrary.org/obo/MONDO_0009669 Werdnig-Hoffmann disease 'Werdnig-Hoffmann disease' SubClassOf 'Proximal spinal muscular atrophy' http://purl.obolibrary.org/obo/MONDO_0044014 postpartum thyroiditis 'postpartum thyroiditis' SubClassOf 'puerperal disorder' 'postpartum thyroiditis' SubClassOf 'autoimmune thyroid disease' 'postpartum thyroiditis' EquivalentTo 'thyroiditis (disease)' and 'puerperal disorder' http://purl.obolibrary.org/obo/MONDO_0019331 rare form of salmonellosis 'rare form of salmonellosis' SubClassOf 'has modifier' some 'rare' 'rare form of salmonellosis' SubClassOf 'bacterial disease' http://purl.obolibrary.org/obo/MONDO_0001592 prolapse of female genital organ 'prolapse of female genital organ' SubClassOf 'female reproductive system disease'