Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q744790-FD137689-581F-475D-B956-B95855AEBE33 P7464 "treacher-collins-syndrome" @default.
- Q749409-D4624CD2-A110-4D27-BDA5-D80AE367179B P7464 "osteogenesis-imperfecta" @default.
- Q7506696-8D12ABB7-32F7-4CA7-928A-9C8A72AD241A P7464 "sialic-acid-storage-disease" @default.
- Q7506696-E75CCBC2-F3BD-4B92-AD8D-1D6D2ECA1B67 P7464 "sialuria" @default.
- Q756289-2FBF54CB-A65B-4EB9-A02C-0B6A8807B360 P7464 "wilms-tumor" @default.
- Q7577467-56247184-E6C3-4791-AF56-DF9FBC61A491 P7464 "spinal-muscular-atrophy-with-lower-extremity-predominance" @default.
- Q7577468-C31C0D35-FAB9-45D1-814C-DEEC34D401EF P7464 "spinal-muscular-atrophy-with-progressive-myoclonic-epilepsy" @default.
- Q7578959-D9F04B9B-F2DF-4C2F-9584-3A28536B65F0 P7464 "spondyloperipheral-dysplasia" @default.
- Q7578960-F98E37F3-BF92-40B0-9FCC-D5C17EF434BB P7464 "spondyloepiphyseal-dysplasia-congenita" @default.
- Q762713-71265C0D-44BE-4D3D-880E-88145746D1B6 P7464 "hypercholesterolemia" @default.
- Q7632698-C511F83B-BB4E-4F22-A2A0-F9B59F36EB8F P7464 "succinyl-coa3-ketoacid-coa-transferase-deficiency" @default.
- Q7706537-7A8BBDF3-6868-430A-B44D-7842CD9BDA06 P7464 "tetrahydrobiopterin-deficiency" @default.
- Q773118-D6EEEF75-AB7F-4D1D-AAE0-789E45CA5ACC P7464 "andersen-tawil-syndrome" @default.
- Q774483-22891C22-3886-44E5-9CEB-59B638751DDD P7464 "galactosemia" @default.
- Q776026-02ABD958-26E9-4FE0-977D-315F09858538 P7464 "biotinidase-deficiency" @default.
- Q776881-85559231-A7DE-414C-8E01-D2A8C1A9F8B4 P7464 "hereditary-hemorrhagic-telangiectasia" @default.
- Q779250-9678A022-80E1-4D41-AAF5-58F0DA403145 P7464 "crouzon-syndrome" @default.
- Q7801152-533D56C6-4620-4298-BB47-19C3773E564C P7464 "tietz-syndrome" @default.
- Q781618-8DD51876-EE57-48C9-A35D-F8954ABDD5C2 P7464 "cleidocranial-dysplasia" @default.
- Q782958-D75E4E7D-F4E2-4CA4-A3FD-792E204B3E3D P7464 "centronuclear-myopathy" @default.
- Q7840696-E842B5BD-97E0-4118-BA9E-C7EFBBB84B74 P7464 "trichohepatoenteric-syndrome" @default.
- Q7876086-DB668487-5871-4CC9-B244-A27918173B40 P7464 "uv-sensitive-syndrome" @default.
- Q787751-20481FC7-F2F2-4E2C-BAAF-E3AAF1728B95 P7464 "glycogen-storage-disease-type-v" @default.
- Q790971-D166B7EE-DFB0-421A-940C-F40871278C0E P7464 "bartter-syndrome" @default.
- Q7925271-9DBAE79A-7278-4090-82FE-98627E20772D P7464 "vici-syndrome" @default.
- Q7939442-CAD615C5-77E1-4F05-84D1-486C73E66ACB P7464 "vohwinkel-syndrome" @default.
- Q8046191-51D13241-02AF-4113-85F3-A3BE63B77D66 P7464 "y-chromosome-infertility" @default.
- Q8277-B1BB39E9-94B8-4FE8-BBAA-85EE0DAE4A6F P7464 "multiple-sclerosis" @default.
- Q8285-D1F8F6B0-396C-4B3A-8167-AA169036DAD5 P7464 "myasthenia-gravis" @default.
- Q829150-693278BF-D871-4859-8FA0-3B001CA1F13C P7464 "glycogen-storage-disease-type-iv" @default.
- Q830265-4E83DE3A-94A5-41F2-8E35-8A62EDAB5796 P7464 "vitelliform-macular-dystrophy" @default.
- Q830308-2F75A113-26F6-4BD1-9692-F035694CECB0 P7464 "age-related-macular-degeneration" @default.
- Q831530-EAC60D4B-9577-4B47-A7C4-2B301D1C16FE P7464 "rosacea" @default.
- Q834047-CC74BA39-9E75-4301-968E-1837193A9AB3 P7464 "schizoaffective-disorder" @default.
- Q844717-A7A1F88F-A61B-4DFF-AA24-9E92903303AC P7464 "spina-bifida" @default.
- Q845779-565AC6A1-C964-4B41-9E24-08A83BD06362 P7464 "fanconi-anemia" @default.
- Q847057-A70B6F6E-2520-4F92-AF47-133AAFB0E7C9 P7464 "retinitis-pigmentosa" @default.
- Q848343-01F7E64D-1956-4762-B2E5-2649E53261C9 P7464 "glucose-6-phosphate-dehydrogenase-deficiency" @default.
- Q852574-472A706E-D6FD-40AE-95E0-570A96FDE624 P7464 "bunion" @default.
- Q858426-B70DE4AB-9BEF-4507-B6E0-1E554D9DCE10 P7464 "5-alpha-reductase-deficiency" @default.
- Q859142-A5F2D947-F06C-4387-B861-12F192B84916 P7464 "citrullinemia" @default.
- Q861224-F4C65FF2-5C35-428C-A199-34BCF4A9C3E2 P7464 "juvenile-idiopathic-arthritis" @default.
- Q861645-36F4FAAA-D05F-4B8E-905F-6D03C6C9D315 P7464 "gaucher-disease" @default.
- Q884590-BA57EEDE-7B52-41AA-A6F7-6159D85C6B5E P7464 "incontinentia-pigmenti" @default.
- Q890470-C46A4449-22B4-40C4-935E-B3F15D16DA0E P7464 "legius-syndrome" @default.
- Q914389-185D4825-84A8-4FAE-9557-4A2E3F219B36 P7464 "cockayne-syndrome" @default.
- Q916280-738F5284-EB6F-439A-9197-ADA19C175354 P7464 "restless-legs-syndrome" @default.
- Q917227-4E1F9293-DAFC-40B8-A5B0-511505B82648 P7464 "sandhoff-disease" @default.
- Q917357-D32AD553-0642-4D8B-BCD7-3FFB996AF364 P7464 "rett-syndrome" @default.
- Q917399-0C9756B2-968A-4DCD-ADCE-EFA82365FD13 P7464 "usher-syndrome" @default.
- Q9182808-25DD3EC3-AFC8-49FB-B8D1-25CA00C9FD83 P7464 "stuve-wiedemann-syndrome" @default.
- Q9190339-0F21E5FA-340B-4308-97F2-FD014F0C2BC1 P7464 "17q12-duplication" @default.
- Q928424-D4FBFD50-0D6A-4E06-8511-7FCBE756C1A4 P7464 "barth-syndrome" @default.
- Q928767-9493EB27-5B32-42E5-A444-6A5A13263B65 P7464 "multiple-familial-trichoepithelioma" @default.
- Q931538-3578666D-CB46-4E88-BFDE-A6AE8D9EBEC1 P7464 "mucolipidosis-type-iv" @default.
- Q9366868-FB2BCC8C-C0B6-4131-ACCF-BB09D10AE6C6 P7464 "generalized-arterial-calcification-of-infancy" @default.
- Q938205-574A532C-2631-4955-B600-D47BF130BC84 P7464 "neuroblastoma" @default.
- Q9390211-6769615A-CDF6-4849-83FA-2E0DB370485C P7464 "branchio-oculo-facial-syndrome" @default.
- Q9390284-3AF380D3-3915-4D87-93FA-40EE4EC5A5D2 P7464 "netherton-syndrome" @default.
- Q9390545-6A163F6B-7A29-4DCB-A9A1-ACE6F5BCA712 P7464 "hyperparathyroidism-jaw-tumor-syndrome" @default.
- Q940210-9F6912B3-2134-4754-8456-75DC1EA6A315 P7464 "ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome" @default.
- Q945930-9233D6E6-0FB1-42F2-A3F5-A8EAA8F23062 P7464 "progressive-supranuclear-palsy" @default.
- Q948318-4CC968D3-95A1-4E93-ABF6-EEC9AF815218 P7464 "polycythemia-vera" @default.
- Q953638-89205732-7865-4F42-A480-E9EA47742A43 P7464 "wiskott-aldrich-syndrome" @default.
- Q959211-052B22FF-4A09-4567-93DC-54C7C222202E P7464 "chylomicron-retention-disease" @default.
- Q97610297-A919AD6B-A19C-417F-8962-8733F12D5ED9 P7464 "syngap1-related-intellectual-disability" @default.
- Q994859-6CF09F3E-F5D6-4D3D-AFCB-5721C8D55012 P7464 "homocystinuria" @default.