Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q5044061-6B69BEE8-6A40-4732-BE44-89ABFBB2D339 P7464 "carnitine-acylcarnitine-translocase-deficiency" @default.
- Q504775-C2AEC43D-816A-4567-B66D-00BF9C627D0A P7464 "bladder-cancer" @default.
- Q5064109-D44DADF3-3297-40AB-A257-38A055A20BE2 P7464 "coats-plus-syndrome" @default.
- Q506433-1D935EEE-6D70-4795-B1F6-52CB28A660DA P7464 "trimethylaminuria" @default.
- Q5075435-97DECF21-3845-42DA-BE5E-3742B883F1EA P7464 "alopecia-areata" @default.
- Q50846110-43D19C55-8046-4FDD-8D80-BCEF13EBEF08 P7464 "hsd10-disease" @default.
- Q510912-FD649F9C-CAD6-4555-B603-E2F7DE75713F P7464 "triple-x-syndrome" @default.
- Q511097-00FC39F8-A03A-40DC-AB68-279A7DD537E9 P7464 "psoriatic-arthritis" @default.
- Q511372-A88A4114-7FC0-4C0A-927E-F7DCF7975474 P7464 "krabbe-disease" @default.
- Q5119339-14209953-6A93-4C61-924B-39312E1243AB P7464 "junctional-epidermolysis-bullosa" @default.
- Q512313-FE65771F-3EAD-470B-96DD-FB9A426B1589 P7464 "androgen-insensitivity-syndrome" @default.
- Q5156399-A1A23FD7-56DA-46DD-AA88-600F985E4A53 P7464 "complement-component-2-deficiency" @default.
- Q5160407-66D1C8D8-FE66-4BE9-BE11-F70C2BB9F97F P7464 "congenital-afibrinogenemia" @default.
- Q5160422-F5678D77-BBAA-43CE-B2FD-F2176BC61D64 P7464 "congenital-dyserythropoietic-anemia" @default.
- Q5160437-9A73B7A5-4732-450F-80D6-58B69FDA0F8D P7464 "congenital-hyperinsulinism" @default.
- Q5198214-044AACE4-F329-4341-A63E-F98650E0C83B P7464 "cyclic-neutropenia" @default.
- Q5203306-844BFD3B-D004-4A41-A29C-D5AA6C18A2C5 P7464 "d-bifunctional-protein-deficiency" @default.
- Q521863-26826939-58C0-43FB-9A17-DDA4B7330428 P7464 "beckwith-wiedemann-syndrome" @default.
- Q5220984-B053272A-6C2C-4F73-AA7E-7A2A69DA4E03 P7464 "danon-disease" @default.
- Q524353-EFAA56BE-6CF1-4B7D-B716-BE75F8C0DA9C P7464 "erythromelalgia" @default.
- Q525642-5c200651-4cad-8986-d6da-4e19b93a816d P7464 "22q112-deletion-syndrome" @default.
- Q5264836-D3A041D2-C859-488D-B077-B3CA9632657E P7464 "desmosterolosis" @default.
- Q5276448-27571020-35CA-4A4F-81E5-4655CE97CEE0 P7464 "dihydropyrimidine-dehydrogenase-deficiency" @default.
- Q52849-4C34C383-27F3-4963-B2DB-DF7EFD195B1A P7464 "ankylosing-spondylitis" @default.
- Q529292-9F448D33-72D0-4E97-B016-F4BB0C1354A0 P7464 "anencephaly" @default.
- Q530142-8247CF7F-BE48-4C08-A1E4-734FE4325EFB P7464 "fg-syndrome" @default.
- Q531012-AEBFAAEE-0900-45DD-8A14-93F64AF5E4C1 P7464 "congenital-hypothyroidism" @default.
- Q5340515-D29838B1-C44D-4885-8B9E-8C72C211325F P7464 "systemic-scleroderma" @default.
- Q535364-48388DBC-3A84-42FB-996A-E486953DD4B3 P7464 "angelman-syndrome" @default.
- Q53660462-30864FEB-CAF8-415D-957F-6C9347932399 P7464 "lysosomal-acid-lipase-deficiency" @default.
- Q5369177-28B025AA-A1E9-4F81-8AE4-9B2BAFD30505 P7464 "emanuel-syndrome" @default.
- Q5375429-B79BAABA-A302-4E24-A5BB-27B5B640FFAA P7464 "ollier-disease" @default.
- Q53951449-AD86FEB2-00BD-4070-9277-5CB8D1CE610E P7464 "dopamine-transporter-deficiency-syndrome" @default.
- Q540571-AC553FB5-E3FB-43D2-8B45-C77527578C14 P7464 "fibromyalgia" @default.
- Q541244-F6B784A4-9979-4562-B653-9CF76A676769 P7464 "hereditary-spherocytosis" @default.
- Q541852-BB0305A6-3086-4ACB-A682-16CDD0E6C653 P7464 "uncombable-hair-syndrome" @default.
- Q5432932-A8A05943-0B10-4A8E-ACA2-B22B0E7AB3D6 P7464 "familial-atrial-fibrillation" @default.
- Q5432935-1CCB259E-69DF-4DB1-8D69-62949CBD5C32 P7464 "familial-encephalopathy-with-neuroserpin-inclusion-bodies" @default.
- Q5432936-FFF544CA-79DF-471E-A958-4E7BA880625D P7464 "familial-exudative-vitreoretinopathy" @default.
- Q5432945-FD753B0D-5982-4515-8F96-2F9CB37A73CA P7464 "familial-partial-lipodystrophy" @default.
- Q5432947-9C7C1A58-5D46-437A-8E3B-9B942B3E3FE2 P7464 "familial-male-limited-precocious-puberty" @default.
- Q543517-C60A779B-17B5-4C7D-8FFC-14EC6E81FCB0 P7464 "juvenile-myoclonic-epilepsy" @default.
- Q5441566-FAA3BF95-04ED-4959-9376-604BE3BB1E8D P7464 "feingold-syndrome" @default.
- Q5463847-A6EB2408-3F65-4DB5-9C82-8CB142F1975F P7464 "focal-dermal-hypoplasia" @default.
- Q548719-4AF8EFF3-AFE7-4F6B-8280-25CCDE4F9EE7 P7464 "aniridia" @default.
- Q548984-AB43AEC4-3375-4220-962A-5708FDCA570B P7464 "dentinogenesis-imperfecta" @default.
- Q5493754-CD2F9C50-6326-475C-9F4A-966558EE752C P7464 "frasier-syndrome" @default.
- Q5513688-90C83E23-B7FF-44F4-9B16-C8782797E646 P7464 "gm2-gangliosidosis-ab-variant" @default.
- Q5514398-01C7D43C-1F59-4C27-B162-3C0D3EEDEF74 P7464 "gracile-syndrome" @default.
- Q5532501-62E24AFD-0A83-4D1C-88FE-94167770A379 P7464 "generalized-pustular-psoriasis" @default.
- Q5533246-4CCBCB45-0254-490A-A310-31DD429B612C P7464 "genitopatellar-syndrome" @default.
- Q55345670-ABF27CEF-DE31-4E4E-8D37-94A401F29DC4 P7464 "autosomal-dominant-optic-atrophy-and-cataract" @default.
- Q55345810-2C4E02E0-D52B-4A4A-86A5-290D2F04BE9A P7464 "autosomal-recessive-cerebellar-ataxia-type-1" @default.
- Q55345816-AD3EA3D2-3404-4E68-BE49-FE0E2E6881D6 P7464 "leukoencephalopathy-with-brainstem-and-spinal-cord-involvement-and-lactate-elevation" @default.
- Q55345866-B54B4E4E-876A-4F9A-BBFD-F33F2D2ECF44 P7464 "leukoencephalopathy-with-thalamus-and-brainstem-involvement-and-high-lactate" @default.
- Q55346074-6258E468-6986-4A9F-840D-0317557C3A2E P7464 "cln4-disease" @default.
- Q5556985-50515B0C-63DA-4AB6-A285-3F5EC2D96D60 P7464 "ghosal-hematodiaphyseal-dysplasia" @default.
- Q5558484-A0BEDD00-1FA2-4244-840B-5DE8027AF4FC P7464 "giant-congenital-melanocytic-nevus" @default.
- Q55603216-5A982938-E8E1-4273-87D2-C8DDA7F50123 P7464 "adenosine-deaminase-2-deficiency" @default.
- Q5560415-19E54EDD-EA28-435A-BACF-54610F39F1E1 P7464 "pulmonary-alveolar-microlithiasis" @default.
- Q5562120-24C44DB9-06CA-450B-8EB2-33521A099881 P7464 "gillespie-syndrome" @default.
- Q5572341-82DCCEB5-6E23-4508-BF2D-576BB7A11F3C P7464 "glucose-galactose-malabsorption" @default.
- Q5572606-51B265A5-4E85-4491-B0AA-D8A0D19328FA P7464 "glycogen-storage-disease-type-0" @default.
- Q55780814-804FB563-258C-4F45-B271-0B8F845AB1D2 P7464 "fibronectin-glomerulopathy" @default.
- Q55781317-D252EA0E-5B52-4537-8BEB-96D2235F11B0 P7464 "osteoglophonic-dysplasia" @default.
- Q55781611-4252CA53-05E4-43D1-9E3A-73D6F635CDE3 P7464 "weyers-acrofacial-dysostosis" @default.
- Q55781796-94E12CB7-8F40-4AA0-A326-C0BD52F3D427 P7464 "renal-hypouricemia" @default.
- Q55781919-037BDDAD-C534-43D1-B493-2FFC6CBB23D2 P7464 "gorlin-chaudhry-moss-syndrome" @default.
- Q55781959-016EC4DA-C936-45B5-99AD-34A8E5B4F17D P7464 "juvenile-paget-disease" @default.
- Q55782066-0CE4DE29-C412-45DD-AF75-D6EED232E431 P7464 "manitoba-oculotrichoanal-syndrome" @default.
- Q55782334-E169C50F-E8E8-4E70-B710-B405F5B0D7C5 P7464 "isolated-sulfite-oxidase-deficiency" @default.
- Q55782468-32284CA1-F02C-4B82-BC27-C5348D9D5723 P7464 "phosphoribosylpyrophosphate-synthetase-superactivity" @default.
- Q55782879-CE21BE93-4DBB-443D-B707-7A56DAAF6DEC P7464 "hyperferritinemia-cataract-syndrome" @default.
- Q55783319-4BD9A636-ADE2-4DEC-BFE1-871E0A94D1A2 P7464 "bosma-arhinia-microphthalmia-syndrome" @default.
- Q55783391-C1DB4D94-4241-4FE4-A841-545EA71BFCAE P7464 "au-kline-syndrome" @default.
- Q55783410-C52F9CDF-2337-4E74-B6FE-F236FA1773C4 P7464 "tyrosine-hydroxylase-deficiency" @default.
- Q55783570-CE7809FA-26BD-47D6-93BD-39CDC98838C8 P7464 "capillary-malformation-arteriovenous-malformation-syndrome" @default.
- Q55783605-A5F34DFB-B8B9-4C14-A89D-AB8E8D21399F P7464 "sudden-infant-death-with-dysgenesis-of-the-testes-syndrome" @default.
- Q55783693-B0E7B7FB-9F24-4722-8DE1-18BE193F1038 P7464 "7q1123-duplication-syndrome" @default.
- Q55783694-DC5AC5D5-B3CF-4B04-8D96-392F65194999 P7464 "acral-peeling-skin-syndrome" @default.
- Q55783762-0652509D-47A4-4EAF-AB9E-A8BBA777D174 P7464 "neutral-lipid-storage-disease-with-myopathy" @default.
- Q55783830-5B63E7F8-90A5-4D2A-B654-6909721F0CFC P7464 "early-onset-myopathy-with-fatal-cardiomyopathy" @default.
- Q55783879-2AD15A01-0F46-438C-A26F-6D88A3E702B4 P7464 "myd88-deficiency" @default.
- Q55783901-BB03D76C-A5CF-423B-915A-A5C6321C00DC P7464 "prekallikrein-deficiency" @default.
- Q55784063-E6C8D269-7C07-48B3-B086-40AE5B77EF00 P7464 "hepatic-lipase-deficiency" @default.
- Q55784267-D073A7D5-B6C6-4313-8DDC-5EEB7350F3CA P7464 "retinal-arterial-macroaneurysm-with-supravalvular-pulmonic-stenosis" @default.
- Q55784418-3F84E70F-D769-4EB4-93CD-3DAE8D406081 P7464 "leptin-receptor-deficiency" @default.
- Q55784600-EB272AAC-929A-46EA-B696-38A6867D04F7 P7464 "hypomyelination-with-brainstem-and-spinal-cord-involvement-and-leg-spasticity" @default.
- Q55784774-9654D02F-00AD-49F7-BCD4-43F4DE5F9A74 P7464 "hereditary-fibrosing-poikiloderma-with-tendon-contractures-myopathy-and-pulmonary-fibrosis" @default.
- Q55784783-F035EFDE-E385-49D8-AF82-FD5B140CF42A P7464 "carbonic-anhydrase-va-deficiency" @default.
- Q55784812-8993D30A-A607-4354-A140-48B12D42A042 P7464 "sting-associated-vasculopathy-with-onset-in-infancy" @default.
- Q55784895-A1199CB9-6758-47F7-92BD-4422A081B4C6 P7464 "chops-syndrome" @default.
- Q55785188-8E5F81E3-9F38-48A5-9773-DDDDC7557DCD P7464 "yao-syndrome" @default.
- Q55787312-7DE491B4-B22C-4199-B8E0-48A35BED7756 P7464 "sialidosis" @default.
- Q55788668-39C8AB98-FC47-4CB8-BCFC-FC5D51B5360D P7464 "lissencephaly-with-cerebellar-hypoplasia" @default.
- Q55789135-7AE8ED6B-BA8A-4039-90ED-C92761056079 P7464 "idiopathic-inflammatory-myopathy" @default.
- Q55790472-3C910761-FA94-4E5B-A1D5-B098E02359DF P7464 "pseudoxanthoma-elasticum" @default.
- Q558077-32B47CB4-EF4D-406C-85EA-800018C17455 P7464 "williams-syndrome" @default.
- Q5598273-C19EA70E-3B02-48D4-B1CA-617D35ED88EA P7464 "gray-platelet-syndrome" @default.
- Q55999489-E45F2E76-0E32-4580-A35A-409AA120B45D P7464 "winchester-syndrome" @default.