Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q187255-BEB89FD5-7DE1-4CF1-B956-7D533F142F5A P7464 "rheumatoid-arthritis" @default.
- Q187542-A66DD977-234C-481F-9CE5-DC59E9709DE8 P7464 "li-fraumeni-syndrome" @default.
- Q1876206-1116E32D-1B56-4F5B-8CDE-61861BE89D54 P7464 "pelizaeus-merzbacher-disease" @default.
- Q187842-8CD25099-6F07-41D5-8C57-9BFE292FD519 P7464 "hashimoto-thyroiditis" @default.
- Q1891209-BCA02A19-AD40-4EE2-AF56-77F3AE869B7F P7464 "mycosis-fungoides" @default.
- Q1892153-BB138C3A-DF09-4D22-B426-BB3D5B24AC26 P7464 "wagr-syndrome" @default.
- Q18932745-AC39996A-9F73-4136-A567-C4C7777D313B P7464 "autosomal-recessive-axonal-neuropathy-with-neuromyotonia" @default.
- Q189561-414491D8-565B-49A2-BE7F-AFC42CA0C5EF P7464 "narcolepsy" @default.
- Q18966102-CB80CFA6-ADA3-4279-89D2-34E949CB3E19 P7464 "baraitser-winter-syndrome" @default.
- Q18966134-D5081A50-0033-4935-8D32-8BD188B23EF2 P7464 "rippling-muscle-disease" @default.
- Q190564-75390709-79ED-4753-9223-9C06EDFF574C P7464 "huntington-disease" @default.
- Q1906054-E050AA74-84D7-4F39-A9C3-45E83AE10209 P7464 "mucopolysaccharidosis-type-i" @default.
- Q1915681-DBD0BECC-B406-4DEF-81F2-CBB46398C9B5 P7464 "meckel-syndrome" @default.
- Q191779-975F20A2-9B92-4DFE-887E-473323E4F1D2 P7464 "tourette-syndrome" @default.
- Q194041-28B9D23B-86A7-41AB-A432-C496CFD87A96 P7464 "phenylketonuria" @default.
- Q1947298-5C26B5B5-339C-490C-B704-EB294AB581F4 P7464 "glycogen-storage-disease-type-vi" @default.
- Q1947307-34A3AE27-AD7F-4EC1-8C6D-79F5367EF1D9 P7464 "primary-familial-brain-calcification" @default.
- Q1951267-D105AD05-771F-4F78-92CD-18AC4EF66CD2 P7464 "moyamoya-disease" @default.
- Q1955377-F147CBBE-FE58-46EF-AB00-9AAA76A47565 P7464 "fukuyama-congenital-muscular-dystrophy" @default.
- Q1958739-F91197D6-494E-4798-8095-B288C91A4366 P7464 "persistent-mullerian-duct-syndrome" @default.
- Q1965082-14D13B55-3DDF-42E6-ACB2-E27F6349043A P7464 "essential-pentosuria" @default.
- Q1995327-FE712EC9-65CB-4A51-A092-F0136C4D633E P7464 "spinal-and-bulbar-muscular-atrophy" @default.
- Q1996246-46155E62-D3D1-44BF-96D2-DF38091BE0BD P7464 "milroy-disease" @default.
- Q200985-5500C451-E1C2-4E1B-A6D2-C9A0A0F14C22 P7464 "hartnup-disease" @default.
- Q2017218-BD3D6755-F719-49E6-B0E0-D2B6BA19D1D8 P7464 "duane-radial-ray-syndrome" @default.
- Q2017741-86930703-A931-49BE-8C8F-192F10F9C24C P7464 "oculocutaneous-albinism" @default.
- Q201989-384C9F5E-AC03-4FD8-88FF-C08931B6415E P7464 "lyme-disease" @default.
- Q2026857-BC02C50F-2C8E-4D61-85AA-96FA913A2476 P7464 "progressive-external-ophthalmoplegia" @default.
- Q202849-D2C17F02-FEC6-4D35-87AB-9F4C290E449C P7464 "turner-syndrome" @default.
- Q2033532-0E5B2622-0D2B-43B7-81BC-7CBB47C081BE P7464 "van-der-woude-syndrome" @default.
- Q2033861-ABCEE613-5F53-40D8-BCA6-CB54880AE769 P7464 "carnitine-palmitoyltransferase-ii-deficiency" @default.
- Q2035074-D24A8EC8-AA2F-473E-B6A0-135D9F8038BA P7464 "paget-disease-of-bone" @default.
- Q205214-1817FBB4-E86C-458E-8EFA-56DD6E55EF9B P7464 "guillain-barre-syndrome" @default.
- Q206901-1C2781FF-556E-49CF-8B51-05AA3E423440 P7464 "amyotrophic-lateral-sclerosis" @default.
- Q207133-9F838A4A-BDFF-4224-96D8-D44217457479 P7464 "klinefelter-syndrome" @default.
- Q208562-8DA23A3D-DAC7-4B0E-B87C-835D6C301EC7 P7464 "marfan-syndrome" @default.
- Q209049-E32C5CA1-4DCA-485D-BCF0-60B316856D63 P7464 "1q211-microdeletion" @default.
- Q2096745-711FDC5E-F294-414A-A8BB-E9BA39CE66A1 P7464 "hereditary-angioedema" @default.
- Q21097778-D63DC442-60CD-4227-A7B3-1161B3CA45EB P7464 "spinocerebellar-ataxia-type-36" @default.
- Q21097855-7D11772A-45CF-4A26-8191-89EB55571B40 P7464 "spinocerebellar-ataxia-type-1" @default.
- Q2110688-BA627EB5-AB03-48EE-8DE7-66C782361C10 P7464 "tetrasomy-18p" @default.
- Q21113887-CF791F1C-E25A-498D-B0AF-2E3731855F9E P7464 "familial-isolated-hyperparathyroidism" @default.
- Q21154055-B2000772-6F97-4328-8E72-530F1ADC25B0 P7464 "10q26-deletion-syndrome" @default.
- Q21154059-B6B72384-D5CC-444D-A75B-05031A6432D9 P7464 "15q24-microdeletion" @default.
- Q21154064-8ECEFCC1-8D68-4B50-9E23-65CB858C399F P7464 "17q12-deletion-syndrome" @default.
- Q2123641-9564C01C-9659-4C93-93CD-35C635E4AE0F P7464 "spondyloepimetaphyseal-dysplasia-strudwick-type" @default.
- Q2142496-49647D60-72E9-4913-9FFE-065596657B2A P7464 "russell-silver-syndrome" @default.
- Q21503282-63FB9B04-6189-4174-BBBC-7F4BF05DBC1C P7464 "episodic-ataxia" @default.
- Q21505516-204380C5-52BA-4047-A2B4-A12D416B938C P7464 "nonsyndromic-congenital-nail-disorder-10" @default.
- Q2160802-DD7D2B7C-CEBE-462A-91DE-C7F6C0735132 P7464 "congenital-nephrotic-syndrome" @default.
- Q2163245-CEAB4E89-D364-4C07-84B6-179EB089A991 P7464 "congenital-diaphragmatic-hernia" @default.
- Q2165663-F2F64EA2-6D23-4F88-8F30-BFD0912D5434 P7464 "chronic-granulomatous-disease" @default.
- Q219223-E88E9E3E-488E-4DC0-83AD-3637C0018D78 P7464 "lactose-intolerance" @default.
- Q2200359-A73F6959-474B-4177-ADDB-00EE0B1D345B P7464 "mucopolysaccharidosis-type-iii" @default.
- Q2214419-FDF1F080-FAE5-46DE-81EF-FA37C23B9D97 P7464 "omenn-syndrome" @default.
- Q221472-C8A1C906-00DE-416A-AB35-47FB0BD991F0 P7464 "fragile-x-syndrome" @default.
- Q22443082-FD8DB14F-F568-4739-987B-FEF061ECBBA7 P7464 "spinocerebellar-ataxia-type-2" @default.
- Q22443772-3C239BB7-B105-4626-9866-E06E259B7F03 P7464 "anonychia-congenita" @default.
- Q2272470-162A4388-C489-4A1E-A73B-3691CC5FAC9F P7464 "carpenter-syndrome" @default.
- Q2288646-81B82806-38B8-47C6-8E68-73C4B2403B9A P7464 "stickler-syndrome" @default.
- Q2290446-BC9D8A49-D71B-466A-9166-63843181E132 P7464 "idiopathic-pulmonary-fibrosis" @default.
- Q2295338-34BBE516-3571-41F1-96A3-4996AFC5DCAA P7464 "smith-magenis-syndrome" @default.
- Q22965506-ED384A00-B7FF-4C60-A194-4D55D455BB65 P7464 "mandibulofacial-dysostosis-with-microcephaly" @default.
- Q2349546-2993C480-8870-4C30-A037-C720937678F0 P7464 "canavan-disease" @default.
- Q23542366-86BD7EB8-2D8A-4B17-828B-4946ECB6E704 P7464 "warsaw-breakage-syndrome" @default.
- Q23542367-339C9B79-6A16-45A1-B167-A43E0488C040 P7464 "mitochondrial-complex-i-deficiency" @default.
- Q2397009-61815ED1-EE8F-42F5-A729-934789FDC522 P7464 "choroideremia" @default.
- Q2406697-96C2E65F-3B20-4789-80E3-0553D8E8B050 P7464 "tetra-amelia-syndrome" @default.
- Q2411095-9E6308A3-D0EB-4903-B883-67751868FA6C P7464 "char-syndrome" @default.
- Q245455-EB8E6D71-A620-4E28-8053-A527A60F2E9F P7464 "5q-minus-syndrome" @default.
- Q2467739-9DB5C298-C675-4845-AB86-802F4F0EC2A3 P7464 "donohue-syndrome" @default.
- Q2470609-23C8D752-E5DA-43DC-9911-026D85404CC8 P7464 "wagner-syndrome" @default.
- Q24975519-48F265CA-809B-4030-8413-B460E45F405A P7464 "warfarin-resistance" @default.
- Q24975607-4A6ED8E6-7422-47F8-BC34-D326DF6E78BA P7464 "mecp2-duplication-syndrome" @default.
- Q2500124-14D43124-703B-476D-904C-FC53E5573FA8 P7464 "lipoid-proteinosis" @default.
- Q250449-0537EBE0-1295-40DB-AB90-8B282C611AA2 P7464 "alpha-mannosidosis" @default.
- Q25098828-22D43985-0E18-49E6-9BD3-04A6463C48C3 P7464 "activated-pi3k-delta-syndrome" @default.
- Q25111656-5944EAFE-8368-4EF4-A55F-E50A5F2AA33B P7464 "xia-gibbs-syndrome" @default.
- Q25324164-876ED341-781D-4DCB-8122-48D37EE154EE P7464 "north-american-indian-childhood-cirrhosis" @default.
- Q25324166-20A36773-08A2-413D-826E-D6A6229A5025 P7464 "isolated-congenital-asplenia" @default.
- Q25324661-9A5F6FA0-EEB0-4943-AF28-2473347CF5D0 P7464 "ataxia-pancytopenia-syndrome" @default.
- Q2532540-A64C324E-6929-4E9C-88A9-C75E8F478EE5 P7464 "birt-hogg-dube-syndrome" @default.
- Q25339349-CB05017A-40E0-4AE8-8F5A-1DDD82220E9D P7464 "familial-hyperaldosteronism" @default.
- Q25381003-95FBD95E-53F6-4F42-8537-E3F888E3C4FC P7464 "x-linked-lissencephaly-with-abnormal-genitalia" @default.
- Q2605012-2B87910A-B579-4DB5-8D2F-79C992A71BAF P7464 "kearns-sayre-syndrome" @default.
- Q2613277-F427B1F8-1C92-4D9F-90BA-165DC70ABD91 P7464 "alpha-thalassemia-x-linked-intellectual-disability-syndrome" @default.
- Q2628677-EF4963D8-149F-4AB2-A02E-E6B49A821289 P7464 "marinesco-sjogren-syndrome" @default.
- Q2632848-7B1C7E29-9D92-4F08-B79C-EC0B20661523 P7464 "alternating-hemiplegia-of-childhood" @default.
- Q265936-CE957218-A32F-48E4-8598-F72136989C29 P7464 "kawasaki-disease" @default.
- Q2666433-A709C0E8-D436-400A-80A5-EF932B9091CD P7464 "mitochondrial-encephalomyopathy-lactic-acidosis-and-stroke-like-episodes" @default.
- Q268667-BFB5869C-0B86-4B14-8BD3-65A4563C0F07 P7464 "atopic-dermatitis" @default.
- Q2691713-93032B19-9D4A-4D78-9361-3B27EC1804EC P7464 "miller-syndrome" @default.
- Q2703116-01311D6A-7EE6-4533-879F-1E609F18C461 P7464 "15q11-q13-duplication-syndrome" @default.
- Q27043982-97F10880-B012-410B-B8A1-3F25E97737A3 P7464 "globozoospermia" @default.
- Q2711291-9AFC4920-069C-45EC-A558-653C1079DD21 P7464 "familial-hypercholesterolemia" @default.
- Q27164415-1AF95E70-AD96-4E36-A687-5D15D09D1E94 P7464 "alpha-methylacyl-coa-racemase-deficiency" @default.
- Q27164424-570EA125-798F-4DAB-ABA4-F2E928134281 P7464 "otulipenia" @default.
- Q271759-AF5F0DD3-DE4B-410D-9BDB-8E632189FBEA P7464 "porphyria" @default.
- Q2735907-3504D4C5-9638-41FB-81F6-CD881716A9AD P7464 "cutis-laxa" @default.
- Q2756703-D7EE6384-9332-41B8-BE39-CA588A9407D0 P7464 "septo-optic-dysplasia" @default.