About: Rare diseases

Property	Value
dbo:wikiPageID	1116081 (xsd:integer)
dbo:wikiPageRevisionID	951653337 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Commons_category dbt:CatAutoTOC dbt:Cat_main dbt:Category_diffuse
rdf:type	skos:Concept
rdfs:label	Rare diseases (en)
skos:broader	dbc:Human_diseases_and_disorders
skos:prefLabel	Rare diseases (en)
prov:wasDerivedFrom	wikipedia-en:Category:Rare_diseases?oldid=951653337&ns=14
is dbo:wikiPageWikiLink of	dbr:Camurati–Engelmann_disease dbr:Canadian_Organization_for_Rare_Disorders dbr:Carcinosarcoma dbr:Caroli_disease dbr:Catecholaminergic_polymorphic_ventricular_tachycardia dbr:Ameloblastic_carcinoma dbr:Benign_hereditary_chorea dbr:Benign_symmetric_lipomatosis dbr:Pre-eclampsia dbr:Pregnancy_and_lactation-associated_osteoporosis dbr:Primary_ciliary_dyskinesia dbr:Progeria dbr:Propionic_acidemia dbr:Pseudohypoparathyroidism dbr:Pulmonary_hypoplasia dbr:Sandhoff_disease dbr:Sanfilippo_syndrome dbr:Schindler_disease dbr:Enterolith dbr:Epidermolysis_bullosa dbr:Epidermolysis_bullosa_acquisita dbr:Epidermolytic_hyperkeratosis dbr:Epispadias dbr:List_of_disorders_included_in_newborn_screening_programs dbr:Necrolytic_migratory_erythema dbr:Nephrogenic_systemic_fibrosis dbr:Neuronal_ceroid_lipofuscinosis dbr:Léri–Weill_dyschondrosteosis dbr:MGUS_polyneuropathy dbr:MURCS_association dbr:Megacystis_(fetal) dbr:Meleda_disease dbr:Melorheostosis dbr:Mendelian_susceptibility_to_mycobacterial_disease dbr:Metachondromatosis dbr:Metachromatic_leukodystrophy dbr:Metaphyseal_dysplasia dbr:Metascreen dbr:Progressive_symmetric_erythrokeratodermia dbr:Omodysplasia_2 dbr:Paroxysmal_exercise-induced_dystonia dbr:Parry–Romberg_syndrome dbr:Wolcott–Rallison_syndrome dbr:Progressive_vaccinia dbr:Procoagulant_platelets dbr:Progressive_pseudorheumatoid_dysplasia dbr:Prolidase_deficiency dbr:Saethre–Chotzen_syndrome dbr:Sarcosinemia dbr:Systemic-onset_juvenile_idiopathic_arthritis dbr:Behçet's_disease dbr:Biotinidase_deficiency dbr:Deficiency_of_the_interleukin-1–receptor_antagonist dbr:Dermatopathia_pigmentosa_reticularis dbr:Anorectal_anomalies dbr:Antithrombin_III_deficiency dbr:Aortopulmonary_septal_defect dbr:Aphallia dbr:Aquagenic_urticaria dbr:Hydranencephaly dbr:Hyperacusis dbr:Hyperekplexia dbr:Hypodysfibrinogenemia dbr:Hypohidrotic_ectodermal_dysplasia dbr:Hypokalemic_periodic_paralysis dbr:Hypoparathyroidism dbr:Hypophosphatasia dbr:Hypopituitarism dbr:Beta-ketothiolase_deficiency dbr:Beta-mannosidosis dbr:Beta_thalassemia dbr:Phakomatosis_pigmentovascularis dbr:Retinoblastoma dbr:Cutis_marmorata_telangiectatica_congenita dbr:Cyclic_neutropenia dbr:Cytochrome_P450_oxidoreductase_deficiency dbr:Cytochrome_b5_deficiency dbr:Umbilical_cord_ulceration_and_intestinal_atresia dbr:Upshaw–Schulman_syndrome dbr:Usher_syndrome dbr:Uveal_melanoma dbr:Vestibular_schwannoma dbr:Von_Hippel–Lindau_disease dbr:Degos_disease dbr:Dejerine–Sottas_disease dbr:Dercum's_disease dbr:Dextrocardia dbr:Donohue_syndrome dbr:Dysfibrinogenemia dbr:EIF5A dbr:Inborn_errors_of_steroid_metabolism dbr:Indium_lung dbr:Infantile_Refsum_disease dbr:Infantile_myofibromatosis dbr:Infantile_neuroaxonal_dystrophy dbr:Iniencephaly dbr:International_Working_Group_on_Neurotransmitter_Related_Disorders dbr:Köhler_disease dbr:Lethal_congenital_contracture_syndrome dbr:Letterer–Siwe_disease dbr:Leukocyte_adhesion_deficiency dbr:Leukocyte_adhesion_deficiency-1 dbr:Leukodystrophy dbr:Leydig_cell_hypoplasia dbr:Lhermitte–Duclos_disease dbr:Waldmann_disease dbr:Pelizaeus–Merzbacher_disease dbr:Pemphigus_foliaceus dbr:Pentasomy_X dbr:Postarthroscopic_glenohumeral_chondrolysis dbr:Postvaccinal_encephalitis dbr:Premature_thelarche dbr:Pseudoaldosteronism dbr:Pseudomyxoma_peritonei dbr:Pseudopseudohypoparathyroidism dbr:Potassium-aggravated_myotonia dbr:Roberts_syndrome dbr:Superficial_siderosis dbr:Villoglandular_adenocarcinoma_of_the_cervix dbr:Wieacker_syndrome dbr:Colloid_cyst dbr:Congenital_insensitivity_to_pain dbr:Congenital_lactic_acidosis dbr:Corticobasal_degeneration dbr:Craniometaphyseal_dysplasia dbr:Creutzfeldt–Jakob_disease dbr:Menkes_disease dbr:Cherubism dbr:Childhood_granulomatous_periorificial_dermatitis dbr:Erythrokeratodermia_variabilis dbr:Erythromelalgia dbr:Erythropoietic_protoporphyria dbr:Gastric_atresia dbr:Genu_recurvatum dbr:Norrie_disease dbr:Ollier_disease dbr:Porokeratosis dbr:Prurigo_pigmentosa dbr:Saccharopinuria dbr:Thumb_hypoplasia dbr:Woodhouse–Sakati_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:Vestigial_twin dbr:Nodding_disease dbr:Vici_syndrome dbr:Rare_disease dbr:Pulmonary_artery_sling dbr:Pulmonary_capillary_hemangiomatosis dbr:Pyknoachondrogenesis dbr:Quadricuspid_aortic_valve dbr:ROHHAD dbr:Scott_syndrome dbr:Seaver_Cassidy_syndrome dbr:Waardenburg_anophthalmia_syndrome dbr:Clouston's_hidrotic_ectodermal_dysplasia dbr:Cockayne_syndrome dbr:Enamel-renal_syndrome dbr:Endocardial_fibroelastosis dbr:Epidermodysplasia_verruciformis dbr:Epidermolysis_bullosa_simplex dbr:Epithelioid_trophoblastic_tumour dbr:GM1_gangliosidoses dbr:GM2_gangliosidoses dbr:Galactose_epimerase_deficiency dbr:Gaucher's_disease dbr:Genetic_Alliance_UK dbr:Gigantism dbr:Glanzmann's_thrombasthenia dbr:Glycogen_storage_disease_type_II dbr:Glycogen_storage_disease_type_VI dbr:Brachydactyly-preaxial_hallux_varus_syndrome dbr:Branched-chain_keto_acid_dehydrogenase_kinase_deficiency dbr:Multiple_epiphyseal_dysplasia dbr:Myotonia_congenita dbr:NGLY1_deficiency dbr:Nail–patella_syndrome dbr:Confluent_and_reticulated_papillomatosis dbr:Congenital_chloride_diarrhea dbr:Congenital_disorder_of_glycosylation_type_IIc dbr:Congenital_ichthyosiform_erythroderma dbr:Congenital_insensitivity_to_pain_with_anhidrosis dbr:Congenital_stromal_corneal_dystrophy dbr:Conjoined_twins dbr:Copenhagen_disease dbr:Cruveilhier–Baumgarten_disease dbr:Erdheim–Chester_disease dbr:LPS-responsive_beige-like_anchor_protein_deficiency dbr:Lafora_disease dbr:Rare_Diseases_Clinical_Research_Network dbr:Sotos_syndrome dbr:True_hermaphroditism dbr:Opitz_G/BBB_syndrome dbr:Organic_acidemia dbr:Ornithine_translocase_deficiency dbr:Osteochondrodysplasia dbr:Otospondylomegaepiphyseal_dysplasia dbr:Anomalous_aortic_origin_of_a_coronary_artery dbr:Antley–Bixler_syndrome dbr:Aposthia dbr:Batten_disease dbr:Legg–Calvé–Perthes_disease dbr:Lethal_arthrogryposis_with_anterior_horn_cell_disease dbr:Leukoencephalopathy_with_vanishing_white_matter dbr:Limb_body_wall_complex dbr:Lipoprotein_lipase_deficiency dbr:Loeys–Dietz_syndrome dbr:Lymphangioleiomyomatosis dbr:Malignant_hyperthermia dbr:Calpainopathy dbr:Chorea-acanthocytosis dbr:Small-cell_carcinoma dbr:Smith–Lemli–Opitz_syndrome dbr:Cleidocranial_dysostosis dbr:Cloacal_exstrophy dbr:Combarros-Calleja-Leno_syndrome dbr:Combined_malonic_and_methylmalonic_aciduria dbr:Dent's_disease dbr:Denys–Drash_syndrome dbr:Zadik–Barak–Levin_syndrome dbr:Zechi-Ceide_syndrome dbr:Zollinger–Ellison_syndrome dbr:Emmonsiosis dbr:Fatal_insomnia dbr:Febrile_neutrophilic_dermatosis dbr:Friedreich's_ataxia dbr:Frontonasal_dysplasia dbr:Fucosidosis dbr:Fukuyama_congenital_muscular_dystrophy dbr:Fumarase_deficiency dbr:Haemolacria dbr:Hailey–Hailey_disease dbr:Hall-Riggs_syndrome dbr:Hallermann–Streiff_syndrome dbr:Harlequin_syndrome dbr:Hemiballismus dbr:Hemihydranencephaly dbr:Hemimegalencephaly dbr:Hemoglobinemia dbr:Ichthyosis dbr:Ichthyosis_bullosa_of_Siemens dbr:Ichthyosis_follicularis_with_alopecia_and_photophobia_syndrome dbr:Ichthyosis_vulgaris dbr:Idiopathic_CD4+_lymphocytopenia dbr:Idiopathic_granulomatous_hepatitis dbr:Idiopathic_sclerosing_mesenteritis dbr:Keratolytic_winter_erythema dbr:Keratomalacia dbr:Kernicterus dbr:Leontiasis_ossea dbr:Uhl_anomaly dbr:Paroxysmal_nocturnal_hemoglobinuria dbr:Pemphigus_vulgaris dbr:Persistent_truncus_arteriosus dbr:Plummer–Vinson_syndrome dbr:Primary_lateral_sclerosis dbr:Progressive_multifocal_leukoencephalopathy dbr:Progressive_rubella_panencephalitis dbr:Progressive_supranuclear_palsy dbr:Pseudohypoaldosteronism dbr:Pulmonary_alveolar_proteinosis dbr:Machado–Joseph_disease dbr:Macrophagic_myofasciitis dbr:Macular_hypoplasia dbr:Malakoplakia dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_1 dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_2A dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_2B dbr:Spitz_nevus dbr:Syrinx_(medicine) dbr:Transverse_myelitis dbr:Treacher_Collins_syndrome dbr:Trigeminal_neuralgia dbr:May–Hegglin_anomaly dbr:Michel_aplasia dbr:Mickleson_syndrome dbr:Microcephalic_primordial_dwarfism,_Montreal_type dbr:Microcephaly_albinism_digital_anomalies_syndrome dbr:Microspherophakia dbr:Microvillous_inclusion_disease dbr:Musical_hallucinations dbr:Musicogenic_epilepsy dbr:Rud_syndrome dbr:Trimethylaminuria dbr:2-Hydroxyglutaric_aciduria dbr:Autosomal_dominant_polycystic_kidney_disease dbr:Brooke_Greenberg dbr:Acute_eosinophilic_pneumonia dbr:Adducted_thumb_syndrome dbr:Adenosine_deaminase_deficiency dbr:Adenosine_monophosphate_deaminase_deficiency_type_1 dbr:Adenylosuccinate_lyase_deficiency dbr:Adermatoglyphia dbr:Adiposis_dolorosa dbr:Adiposogenital_dystrophy dbr:Adipsia dbr:Thrombotic_thrombocytopenic_purpura dbr:Thyroid_hormone_resistance dbr:Tracheobronchomalacia dbr:Trichothiodystrophy dbr:Tuberous_sclerosis
is dcterms:subject of	dbr:Camurati–Engelmann_disease dbr:Canadian_Organization_for_Rare_Disorders dbr:Carcinosarcoma dbr:Caroli_disease dbr:Catecholaminergic_polymorphic_ventricular_tachycardia dbr:Ameloblastic_carcinoma dbr:Benign_hereditary_chorea dbr:Benign_symmetric_lipomatosis dbr:Pre-eclampsia dbr:Pregnancy_and_lactation-associated_osteoporosis dbr:Primary_ciliary_dyskinesia dbr:Progeria dbr:Propionic_acidemia dbr:Pseudohypoparathyroidism dbr:Pulmonary_hypoplasia dbr:Sandhoff_disease dbr:Sanfilippo_syndrome dbr:Schindler_disease dbr:Enterolith dbr:Epidermolysis_bullosa dbr:Epidermolysis_bullosa_acquisita dbr:Epidermolytic_hyperkeratosis dbr:Epispadias dbr:List_of_disorders_included_in_newborn_screening_programs dbr:Necrolytic_migratory_erythema dbr:Nephrogenic_systemic_fibrosis dbr:Neuronal_ceroid_lipofuscinosis dbr:Léri–Weill_dyschondrosteosis dbr:MGUS_polyneuropathy dbr:MURCS_association dbr:Megacystis_(fetal) dbr:Meleda_disease dbr:Melorheostosis dbr:Mendelian_susceptibility_to_mycobacterial_disease dbr:Metachondromatosis dbr:Metachromatic_leukodystrophy dbr:Metaphyseal_dysplasia dbr:Metascreen dbr:Progressive_symmetric_erythrokeratodermia dbr:Omodysplasia_2 dbr:Paroxysmal_exercise-induced_dystonia dbr:Parry–Romberg_syndrome dbr:Wolcott–Rallison_syndrome dbr:Progressive_vaccinia dbr:Procoagulant_platelets dbr:Progressive_pseudorheumatoid_dysplasia dbr:Prolidase_deficiency dbr:Saethre–Chotzen_syndrome dbr:Sarcosinemia dbr:Systemic-onset_juvenile_idiopathic_arthritis dbr:Behçet's_disease dbr:Biotinidase_deficiency dbr:Deficiency_of_the_interleukin-1–receptor_antagonist dbr:Dermatopathia_pigmentosa_reticularis dbr:Anorectal_anomalies dbr:Antithrombin_III_deficiency dbr:Aortopulmonary_septal_defect dbr:Aphallia dbr:Aquagenic_urticaria dbr:Hydranencephaly dbr:Hyperacusis dbr:Hyperekplexia dbr:Hypodysfibrinogenemia dbr:Hypohidrotic_ectodermal_dysplasia dbr:Hypokalemic_periodic_paralysis dbr:Hypoparathyroidism dbr:Hypophosphatasia dbr:Hypopituitarism dbr:Beta-ketothiolase_deficiency dbr:Beta-mannosidosis dbr:Beta_thalassemia dbr:Phakomatosis_pigmentovascularis dbr:Retinoblastoma dbr:Cutis_marmorata_telangiectatica_congenita dbr:Cyclic_neutropenia dbr:Cytochrome_P450_oxidoreductase_deficiency dbr:Cytochrome_b5_deficiency dbr:Umbilical_cord_ulceration_and_intestinal_atresia dbr:Upshaw–Schulman_syndrome dbr:Usher_syndrome dbr:Uveal_melanoma dbr:Vestibular_schwannoma dbr:Von_Hippel–Lindau_disease dbr:Degos_disease dbr:Dejerine–Sottas_disease dbr:Dercum's_disease dbr:Dextrocardia dbr:Donohue_syndrome dbr:Dysfibrinogenemia dbr:EIF5A dbr:Inborn_errors_of_steroid_metabolism dbr:Indium_lung dbr:Infantile_Refsum_disease dbr:Infantile_myofibromatosis dbr:Infantile_neuroaxonal_dystrophy dbr:Iniencephaly dbr:International_Working_Group_on_Neurotransmitter_Related_Disorders dbr:Köhler_disease dbr:Lethal_congenital_contracture_syndrome dbr:Letterer–Siwe_disease dbr:Leukocyte_adhesion_deficiency dbr:Leukocyte_adhesion_deficiency-1 dbr:Leukodystrophy dbr:Leydig_cell_hypoplasia dbr:Lhermitte–Duclos_disease dbr:Waldmann_disease dbr:Pelizaeus–Merzbacher_disease dbr:Pemphigus_foliaceus dbr:Pentasomy_X dbr:Postarthroscopic_glenohumeral_chondrolysis dbr:Postvaccinal_encephalitis dbr:Premature_thelarche dbr:Pseudoaldosteronism dbr:Pseudomyxoma_peritonei dbr:Pseudopseudohypoparathyroidism dbr:Potassium-aggravated_myotonia dbr:Roberts_syndrome dbr:Superficial_siderosis dbr:Villoglandular_adenocarcinoma_of_the_cervix dbr:Wieacker_syndrome dbr:Colloid_cyst dbr:Congenital_insensitivity_to_pain dbr:Congenital_lactic_acidosis dbr:Corticobasal_degeneration dbr:Craniometaphyseal_dysplasia dbr:Creutzfeldt–Jakob_disease dbr:Menkes_disease dbr:Cherubism dbr:Childhood_granulomatous_periorificial_dermatitis dbr:Erythrokeratodermia_variabilis dbr:Erythromelalgia dbr:Erythropoietic_protoporphyria dbr:Gastric_atresia dbr:Genu_recurvatum dbr:Norrie_disease dbr:Ollier_disease dbr:Porokeratosis dbr:Prurigo_pigmentosa dbr:Saccharopinuria dbr:Thumb_hypoplasia dbr:Woodhouse–Sakati_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:Vestigial_twin dbr:Nodding_disease dbr:Vici_syndrome dbr:Rare_disease dbr:Pulmonary_artery_sling dbr:Pulmonary_capillary_hemangiomatosis dbr:Pyknoachondrogenesis dbr:Quadricuspid_aortic_valve dbr:ROHHAD dbr:Scott_syndrome dbr:Seaver_Cassidy_syndrome dbr:Waardenburg_anophthalmia_syndrome dbr:Clouston's_hidrotic_ectodermal_dysplasia dbr:Cockayne_syndrome dbr:Enamel-renal_syndrome dbr:Endocardial_fibroelastosis dbr:Epidermodysplasia_verruciformis dbr:Epidermolysis_bullosa_simplex dbr:Epithelioid_trophoblastic_tumour dbr:GM1_gangliosidoses dbr:GM2_gangliosidoses dbr:Galactose_epimerase_deficiency dbr:Gaucher's_disease dbr:Genetic_Alliance_UK dbr:Gigantism dbr:Glanzmann's_thrombasthenia dbr:Glycogen_storage_disease_type_II dbr:Glycogen_storage_disease_type_VI dbr:Brachydactyly-preaxial_hallux_varus_syndrome dbr:Branched-chain_keto_acid_dehydrogenase_kinase_deficiency dbr:Multiple_epiphyseal_dysplasia dbr:Myotonia_congenita dbr:NGLY1_deficiency dbr:Nail–patella_syndrome dbr:Confluent_and_reticulated_papillomatosis dbr:Congenital_chloride_diarrhea dbr:Congenital_disorder_of_glycosylation_type_IIc dbr:Congenital_ichthyosiform_erythroderma dbr:Congenital_insensitivity_to_pain_with_anhidrosis dbr:Congenital_stromal_corneal_dystrophy dbr:Conjoined_twins dbr:Copenhagen_disease dbr:Cruveilhier–Baumgarten_disease dbr:Erdheim–Chester_disease dbr:LPS-responsive_beige-like_anchor_protein_deficiency dbr:Lafora_disease dbr:Rare_Diseases_Clinical_Research_Network dbr:Sotos_syndrome dbr:True_hermaphroditism dbr:Opitz_G/BBB_syndrome dbr:Organic_acidemia dbr:Ornithine_translocase_deficiency dbr:Osteochondrodysplasia dbr:Otospondylomegaepiphyseal_dysplasia dbr:Anomalous_aortic_origin_of_a_coronary_artery dbr:Antley–Bixler_syndrome dbr:Aposthia dbr:Batten_disease dbr:Legg–Calvé–Perthes_disease dbr:Lethal_arthrogryposis_with_anterior_horn_cell_disease dbr:Leukoencephalopathy_with_vanishing_white_matter dbr:Limb_body_wall_complex dbr:Lipoprotein_lipase_deficiency dbr:Loeys–Dietz_syndrome dbr:Lymphangioleiomyomatosis dbr:Malignant_hyperthermia dbr:Calpainopathy dbr:Chorea-acanthocytosis dbr:Small-cell_carcinoma dbr:Smith–Lemli–Opitz_syndrome dbr:Cleidocranial_dysostosis dbr:Cloacal_exstrophy dbr:Combarros-Calleja-Leno_syndrome dbr:Combined_malonic_and_methylmalonic_aciduria dbr:Dent's_disease dbr:Denys–Drash_syndrome dbr:Zadik–Barak–Levin_syndrome dbr:Zechi-Ceide_syndrome dbr:Zollinger–Ellison_syndrome dbr:Emmonsiosis dbr:Fatal_insomnia dbr:Febrile_neutrophilic_dermatosis dbr:Friedreich's_ataxia dbr:Frontonasal_dysplasia dbr:Fucosidosis dbr:Fukuyama_congenital_muscular_dystrophy dbr:Fumarase_deficiency dbr:Haemolacria dbr:Hailey–Hailey_disease dbr:Hall-Riggs_syndrome dbr:Hallermann–Streiff_syndrome dbr:Harlequin_syndrome dbr:Hemiballismus dbr:Hemihydranencephaly dbr:Hemimegalencephaly dbr:Hemoglobinemia dbr:Ichthyosis dbr:Ichthyosis_bullosa_of_Siemens dbr:Ichthyosis_follicularis_with_alopecia_and_photophobia_syndrome dbr:Ichthyosis_vulgaris dbr:Idiopathic_CD4+_lymphocytopenia dbr:Idiopathic_granulomatous_hepatitis dbr:Idiopathic_sclerosing_mesenteritis dbr:Keratolytic_winter_erythema dbr:Keratomalacia dbr:Kernicterus dbr:Leontiasis_ossea dbr:Uhl_anomaly dbr:Paroxysmal_nocturnal_hemoglobinuria dbr:Pemphigus_vulgaris dbr:Persistent_truncus_arteriosus dbr:Plummer–Vinson_syndrome dbr:Primary_lateral_sclerosis dbr:Progressive_multifocal_leukoencephalopathy dbr:Progressive_rubella_panencephalitis dbr:Progressive_supranuclear_palsy dbr:Pseudohypoaldosteronism dbr:Pulmonary_alveolar_proteinosis dbr:Machado–Joseph_disease dbr:Macrophagic_myofasciitis dbr:Macular_hypoplasia dbr:Malakoplakia dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_1 dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_2A dbr:Spinal_muscular_atrophy_with_lower_extremity_predominance_2B dbr:Spitz_nevus dbr:Syrinx_(medicine) dbr:Transverse_myelitis dbr:Treacher_Collins_syndrome dbr:Trigeminal_neuralgia dbr:May–Hegglin_anomaly dbr:Michel_aplasia dbr:Mickleson_syndrome dbr:Microcephalic_primordial_dwarfism,_Montreal_type dbr:Microcephaly_albinism_digital_anomalies_syndrome dbr:Microspherophakia dbr:Microvillous_inclusion_disease dbr:Musical_hallucinations dbr:Musicogenic_epilepsy dbr:Rud_syndrome dbr:Trimethylaminuria dbr:2-Hydroxyglutaric_aciduria dbr:Autosomal_dominant_polycystic_kidney_disease dbr:Brooke_Greenberg dbr:Acute_eosinophilic_pneumonia dbr:Adducted_thumb_syndrome dbr:Adenosine_deaminase_deficiency dbr:Adenosine_monophosphate_deaminase_deficiency_type_1 dbr:Adenylosuccinate_lyase_deficiency dbr:Adermatoglyphia dbr:Adiposis_dolorosa dbr:Adiposogenital_dystrophy dbr:Adipsia dbr:Thrombotic_thrombocytopenic_purpura dbr:Thyroid_hormone_resistance dbr:Tracheobronchomalacia dbr:Trichothiodystrophy dbr:Tuberous_sclerosis
is skos:broader of	dbc:Deaths_from_scleroderma dbc:Intersex_and_medicine dbc:People_with_hypertrichosis dbc:Supernumerary_body_parts dbc:Absent_body_parts dbc:Deaths_from_thrombotic_thrombocytopenic_purpura dbc:Arthrogryposis dbc:Motor_neuron_diseases dbc:People_with_tetra-amelia_syndrome dbc:Intersex_variations dbc:People_with_caudal_regression_syndrome dbc:Mesothelioma dbc:Mitochondrial_diseases dbc:Rare_syndromes dbc:Cystic_fibrosis dbc:Amyotrophic_lateral_sclerosis dbc:Rare_cancers dbc:Rare_infectious_diseases dbc:Progeroid_syndromes dbc:Fibrodysplasia_ossificans_progressiva dbc:Tay–Sachs_disease