Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q3508576-C5393C51-B955-4E13-B15A-C42FB3796EE1 P7464 "neuropathy-ataxia-and-retinitis-pigmentosa" @default.
- Q3508578-50B5214A-024A-4D5F-BDF7-7DCB6EE9EFEC P7464 "rapadilino-syndrome" @default.
- Q3508595-A71B96AB-2DB8-4327-BFE7-27A787F76ED5 P7464 "andermann-syndrome" @default.
- Q3508618-DA0E7B7C-BD30-4E06-A462-6F88140E3F52 P7464 "congenital-contractural-arachnodactyly" @default.
- Q3508635-BF8FB21C-43AE-453C-8EB0-F6A51DFDDEF3 P7464 "fryns-syndrome" @default.
- Q3508649-70E5EA43-604E-47EF-8B92-BBA419653275 P7464 "greig-cephalopolysyndactyly-syndrome" @default.
- Q3508679-3144A20B-AE80-4FA8-ACF8-5481ADD18481 P7464 "muenke-syndrome" @default.
- Q3508705-5DFEA770-9B4B-4BBC-AFC0-68C65ACC346C P7464 "timothy-syndrome" @default.
- Q3508706-9EA1C909-5CCC-4F4A-AE61-22C5492CE013 P7464 "troyer-syndrome" @default.
- Q3508750-7A3BEDA0-A03B-40BA-9633-15DA1DCC0A07 P7464 "opitz-g-bbb-syndrome" @default.
- Q3508764-571FE924-F545-417C-83BF-979B1F9E8F76 P7464 "hand-foot-genital-syndrome" @default.
- Q3508768-E097ED5F-022A-4917-991B-9AF7801E54B8 P7464 "lymphedema-distichiasis-syndrome" @default.
- Q3508783-2F1E208F-9CDB-4ABD-BABD-C0B4DD78155A P7464 "oral-facial-digital-syndrome" @default.
- Q3508795-9728CDA9-7216-4106-B461-FFE8EAF2CD9C P7464 "trichorhinophalangeal-syndrome-type-ii" @default.
- Q3508800-BB562A62-E13A-486D-9885-A920278534E1 P7464 "congenital-myasthenic-syndrome" @default.
- Q3512243-4C81F8FA-FBA2-41F7-A91C-A630969EA9BB P7464 "tumor-necrosis-factor-receptor-associated-periodic-syndrome" @default.
- Q3539030-033DAB1A-DDE7-49F0-86C7-6BB512F96DED P7464 "trichothiodystrophy" @default.
- Q356410-F284EC9B-754F-4F5D-9F6D-1B9552DFC594 P7464 "adermatoglyphia" @default.
- Q3567797-43671ECC-5E48-4D87-9876-062EE0A1A679 P7464 "white-sponge-nevus" @default.
- Q3589131-EF117877-9C91-441D-B803-52F3EB3663F1 P7464 "dystrophic-epidermolysis-bullosa" @default.
- Q3589157-0EC3A5B9-69D8-4F07-9C82-A8C613F40672 P7464 "autosomal-dominant-nocturnal-frontal-lobe-epilepsy" @default.
- Q3591493-7779B01D-6976-47D7-BA19-A68E41D3F4FF P7464 "erythrokeratodermia-variabilis-et-progressiva" @default.
- Q3616632-9212E209-9B1B-45B2-B0CB-A3C919EE57F0 P7464 "beta-thalassemia" @default.
- Q365589-E30A6BF4-CA6A-4231-92BA-B1EB7409D91B P7464 "46xx-testicular-disorder-of-sex-development" @default.
- Q36956-C24E52A1-4643-4CE5-A471-C0A1F2259A96 P7464 "leprosy" @default.
- Q3702898-F69454D8-1E4B-4580-B0E5-5219BDEA39E6 P7464 "familial-dysautonomia" @default.
- Q3709312-92CA4A04-8C90-43DD-B8DD-13E88BE0D9B2 P7464 "dyskeratosis-congenita" @default.
- Q3710440-2DFB8635-D113-41A8-8BC8-FA9122BD3876 P7464 "myoclonus-dystonia" @default.
- Q3725646-424A9BF3-69FF-46C1-8800-32EEBBA7C487 P7464 "frontonasal-dysplasia" @default.
- Q3731836-3D24AC85-6C2C-4956-8043-4DE6D7AF2E5A P7464 "lamellar-ichthyosis" @default.
- Q3731836-90B025DD-BDBD-4B0A-9352-926DA97B275B P7464 "nonbullous-congenital-ichthyosiform-erythroderma" @default.
- Q374036-E90571D5-B500-4B84-967E-DB57CC8AE992 P7464 "langerhans-cell-histiocytosis" @default.
- Q379038-9A60AFF1-32D0-444A-A46C-43B97B143AA5 P7464 "adult-polyglucosan-body-disease" @default.
- Q3801491-4D9A1416-5BA6-485B-907F-1819AB7C7790 P7464 "epidermolytic-hyperkeratosis" @default.
- Q3843790-9930131F-C587-4B42-ABC8-78C7653DF8E9 P7464 "myh9-related-disorder" @default.
- Q3851644-6AD89902-9D8D-46AE-ACB7-A3F5F788170C P7464 "systemic-mastocytosis" @default.
- Q3857106-949F48AC-AC3D-451D-A50A-23EA4695C6AD P7464 "primary-myelofibrosis" @default.
- Q3924862-5E51957E-0457-49A1-B4A2-5336ED6511B4 P7464 "intestinal-pseudo-obstruction" @default.
- Q3961685-BF7A8F38-AB03-4036-A238-30FEF62127DD P7464 "rabson-mendenhall-syndrome" @default.
- Q39656409-BEF18445-AB33-47B9-BC5A-3AA34B50FBD5 P7464 "potocki-lupski-syndrome" @default.
- Q3972207-A7119940-E0EE-4266-A70E-C269EC2B64B4 P7464 "steatocystoma-multiplex" @default.
- Q402575-BE97D5F4-80D1-4C97-823F-4EB040B22AD5 P7464 "maple-syrup-urine-disease" @default.
- Q402575-DAED3B6A-8463-4D97-A0FF-E1D6016B947B P7464 "dihydrolipoamide-dehydrogenase-deficiency" @default.
- Q403453-CCDF76AA-62D2-4B49-8C14-C6D6BC600681 P7464 "aicardi-goutieres-syndrome" @default.
- Q403463-C3DDEF12-4941-4611-A7F3-FD243BD76E9B P7464 "aicardi-syndrome" @default.
- Q4052543-2438F916-D18D-457D-9DEE-8DD56A483F4D P7464 "vldlr-associated-cerebellar-hypoplasia" @default.
- Q41112-130B1E97-59CB-4B87-9CE2-9F6299CDB185 P7464 "schizophrenia" @default.
- Q4127187-A4BB2F4A-B605-46E6-BB69-176898826B8D P7464 "congenital-stromal-corneal-dystrophy" @default.
- Q4162392-806C958E-21D5-4329-9957-07305AA7B9F0 P7464 "meesmann-corneal-dystrophy" @default.
- Q41861-B327E06B-521B-4E15-BEC0-2ADD54F0C921 P7464 "hypertension" @default.
- Q4216194-3012F505-0C17-4192-84FD-BA43FEF95B34 P7464 "arterial-tortuosity-syndrome" @default.
- Q42844-869F3936-A684-47C0-8DAC-09A07C81136E P7464 "depression" @default.
- Q4293116-235841C3-AA57-48F4-A5E2-F22F17E54F9E P7464 "microvillus-inclusion-disease" @default.
- Q432396-0C9BCECD-91D6-40CC-9FC8-35C341DAE98C P7464 "achromatopsia" @default.
- Q432814-E4622393-9605-4543-85D8-94D78B7806B0 P7464 "alstrom-syndrome" @default.
- Q4348144-6B600DF0-CAAF-4425-862A-61AEAE9B1D31 P7464 "weaver-syndrome" @default.
- Q4352832-B6AE111D-2317-45A4-8AF2-6A2390A948F9 P7464 "ochoa-syndrome" @default.
- Q4354267-C2457241-9765-4D59-9DDF-51A7E4F42083 P7464 "senior-loken-syndrome" @default.
- Q441077-984672F7-36F5-4634-9159-9C02A35561EA P7464 "blau-syndrome" @default.
- Q4412533-0FBC61DE-E753-48A0-85F5-F07C41819DCE P7464 "aspartylglucosaminuria" @default.
- Q4420136-A3F89813-0ED5-4F18-A6F5-883FC7627810 P7464 "multicentric-osteolysis-nodulosis-and-arthropathy" @default.
- Q4553565-5DBFA9CB-BBFE-4959-B918-32C51FD821E1 P7464 "koolen-de-vries-syndrome" @default.
- Q457737-510EC367-D89D-434F-AD96-FEE5ED5BB4E3 P7464 "trisomy-18" @default.
- Q458099-60AE4AE7-3F63-4935-982C-5E57AEDE0A13 P7464 "triosephosphate-isomerase-deficiency" @default.
- Q4596905-336D3714-11E2-4E4A-BEF0-8514AB25B8EF P7464 "short-branched-chain-acyl-coa-dehydrogenase-deficiency" @default.
- Q461854-AE362246-68C7-46EC-AC2E-B2025EF95E09 P7464 "amelogenesis-imperfecta" @default.
- Q4636618-9CAF93CD-D439-4F1B-915B-38D582B882B9 P7464 "3q29-microdeletion-syndrome" @default.
- Q4675304-52B9C75B-8CBA-48AB-9121-EA8E062CEC57 P7464 "acrocallosal-syndrome" @default.
- Q4676182-D4D59316-4FD7-417E-B649-33F0CF832B2D P7464 "acromicric-dysplasia" @default.
- Q467635-47F55C50-12E6-4CFA-B99E-70538DF9797B P7464 "multiple-myeloma" @default.
- Q4682223-F2B0A9D1-5B5E-4EB3-B4F8-EA3018483E0B P7464 "adenine-phosphoribosyltransferase-deficiency" @default.
- Q4682317-28838805-51A4-40C5-8467-AA499F73C482 P7464 "adenylosuccinate-lyase-deficiency" @default.
- Q4690019-A766DF2B-F9FB-4900-BC88-1B9D2B8AEA1C P7464 "african-iron-overload" @default.
- Q474237-F63A5AC5-B105-45D4-9C71-211BE55A33B2 P7464 "distal-18q-deletion-syndrome" @default.
- Q475086-1EA551D7-E7CB-4CD0-B598-7604B12CD83E P7464 "desmoid-tumor" @default.
- Q47715-6125DD09-3742-4473-8BE5-6284637BBB94 P7464 "down-syndrome" @default.
- Q47912-6FF40574-A3DB-4DD1-BCD0-3021B33BEDEC P7464 "lung-cancer" @default.
- Q4795506-5C11D61E-50E3-4261-B889-F203C2ABAAE8 P7464 "aromatase-deficiency" @default.
- Q4795508-43B9B267-6300-40A7-B6AF-4358B5921004 P7464 "aromatase-excess-syndrome" @default.
- Q4807981-85B31F64-256C-4BA4-9DEE-FB80862AE85B P7464 "asphyxiating-thoracic-dystrophy" @default.
- Q4821698-B9D3E9C0-BA02-4BC2-B25F-EB73BAEE526A P7464 "spondylocostal-dysostosis" @default.
- Q4821698-DB112D22-5B58-4B12-A2B5-C17492430B65 P7464 "spondylothoracic-dysostosis" @default.
- Q48340195-0D2E1E22-10AF-4DD6-AB81-DA2FF9D5B0D5 P7464 "glutamate-formiminotransferase-deficiency" @default.
- Q4897218-AD60806D-BCA9-458C-AF6C-9C2C6618E0A5 P7464 "beta-ketothiolase-deficiency" @default.
- Q4904691-B87D464C-AC14-446E-8A7E-D6951C1404F8 P7464 "bietti-crystalline-dystrophy" @default.
- Q4919794-E247647D-12F6-40C3-A2FD-171703F0D441 P7464 "bjornstad-syndrome" @default.
- Q493103-6FA528E6-CEB2-4193-967F-3583E022685D P7464 "paramyotonia-congenita" @default.
- Q4943512-1FD9B604-5536-4E6F-8720-C0E0F4B11531 P7464 "boomerang-dysplasia" @default.
- Q494922-87C14893-A8E8-445B-8278-D350B72554C4 P7464 "glycogen-storage-disease-type-iii" @default.
- Q4973199-DD462FEB-AB6F-41F4-A44C-1429964C7143 P7464 "brody-myopathy" @default.
- Q498487-6679036E-0EFA-4D17-9F12-44DDDD6AB7DF P7464 "camurati-engelmann-disease" @default.
- Q4990874-A7D6669F-D183-4A7F-8B80-06749658D994 P7464 "congenital-fibrosis-of-the-extraocular-muscles" @default.
- Q500695-04826BC3-8F98-4607-A2A8-DE8393A1A87E P7464 "retinoblastoma" @default.
- Q500816-11BA5AD6-8984-499A-B003-0ED901DC95E8 P7464 "polycystic-ovary-syndrome" @default.
- Q501694-B5146AB6-C1A8-4445-9971-1427162F1AB0 P7464 "congenital-insensitivity-to-pain-with-anhidrosis" @default.
- Q5034093-CAA08D17-3E9C-4F60-9D26-88A9170E31B5 P7464 "cantu-syndrome" @default.
- Q50349727-89099D09-5711-48B6-B3F6-C34A57D0D79F P7464 "hereditary-sensory-and-autonomic-neuropathy-type-ii" @default.
- Q50349805-3A1A4157-EB80-42ED-A94F-1A115AB10CFD P7464 "mitochondrial-complex-iii-deficiency" @default.
- Q50349837-6DF575A2-6CE6-480B-BCE2-7BF658632ABF P7464 "subcortical-band-heterotopia" @default.
- Q5037834-9E540FA9-67E9-4BCF-8CBE-4B94C85BB168 P7464 "carbamoyl-phosphate-synthetase-i-deficiency" @default.