Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q2757585-6C5BAB15-2FC8-4361-A99C-A771BB804101 P7464 "mowat-wilson-syndrome" @default.
- Q27677577-C46D8793-779C-4A89-A872-0FBCC043A122 P7464 "megdel-syndrome" @default.
- Q27835675-B052ADE0-452A-456A-A79A-A9B496BEA85E P7464 "lmna-related-congenital-muscular-dystrophy" @default.
- Q28065590-21909B0D-B273-4E41-941C-1917A7FDD9DE P7464 "autosomal-dominant-leukodystrophy-with-autonomic-disease" @default.
- Q28065598-1E25219B-B324-45A6-90EC-750189B5E67A P7464 "hypomyelination-and-congenital-cataract" @default.
- Q28065629-89C9FA5C-F788-4E8C-92B2-5E96B75A120A P7464 "christianson-syndrome" @default.
- Q28065631-027939AC-7E97-4826-A2A9-FFBCB236C116 P7464 "ppm-x-syndrome" @default.
- Q281115-DC5FDF19-BEAD-4CA4-9C38-7AC60238868C P7464 "proteus-syndrome" @default.
- Q28208917-BECD31BF-75FF-4492-A9F2-57DD00D29444 P7464 "aminoacylase-1-deficiency" @default.
- Q2823145-F57AA541-697B-4E51-AA42-CDCDA4831E17 P7464 "achondrogenesis" @default.
- Q2823332-E685CFB0-07D7-438C-A8B5-C7266480E0B7 P7464 "costeff-syndrome" @default.
- Q2823333-C072ADD6-B4CA-45CA-B798-2C107F08DDD7 P7464 "succinic-semialdehyde-dehydrogenase-deficiency" @default.
- Q2823337-6489D395-0F44-4BF6-AA44-A18055D94DEA P7464 "fumarase-deficiency" @default.
- Q283108-9497DE43-C5AC-4D19-9CEF-2F6D00D01E82 P7464 "x-linked-agammaglobulinemia" @default.
- Q2831905-3EF3636D-0C54-49F2-9412-5568B709779B P7464 "ocular-albinism" @default.
- Q284219-7DF1E9E9-5723-47A2-8AD4-37044B37E8D8 P7464 "trisomy-13" @default.
- Q2852251-F466EC0B-E262-4D35-9D8D-9BA42831A3A0 P7464 "abdominal-wall-defect" @default.
- Q2868786-3BA3831E-6A9C-4A2A-B0AA-D0C8E7C5FD36 P7464 "autosomal-recessive-spastic-ataxia-of-charlevoix-saguenay" @default.
- Q2868788-8B917BDA-261D-499A-89A7-11C676F0D7E9 P7464 "spinocerebellar-ataxia-type-6" @default.
- Q2869820-1ACB290E-4B90-41D5-A9DB-F8E5B3F15B69 P7464 "optic-atrophy-type-1" @default.
- Q2892779-C9A4A08B-9817-45E5-9526-434A79134149 P7464 "nephrogenic-diabetes-insipidus" @default.
- Q2894827-E61746FC-0476-4767-BF8D-5C9EE0D9A945 P7464 "childhood-absence-epilepsy" @default.
- Q29014971-56A723A4-942B-4E94-AA9F-2014E28308A4 P7464 "auriculo-condylar-syndrome" @default.
- Q291617-7C24F9B6-BF3C-450F-A840-5A21C294C4CD P7464 "beta-mannosidosis" @default.
- Q2936204-5B07DF96-1ECC-43DE-999D-36B6673408D9 P7464 "hereditary-diffuse-gastric-cancer" @default.
- Q2966732-758B6E1E-0FDB-473F-B670-14C33F58F67A P7464 "ring-chromosome-14-syndrome" @default.
- Q2966733-07DC5D39-351C-45AF-9852-4FCC41A7B1A5 P7464 "ring-chromosome-20-syndrome" @default.
- Q2991265-65689E96-71FF-4E5F-93CF-0375C796B7E4 P7464 "polymicrogyria" @default.
- Q29982053-4F528EFA-D170-47E2-9F0E-18A23F33B13F P7464 "otopalatodigital-syndrome-type-2" @default.
- Q29982088-C3658F1C-753C-4B87-A5DD-DD9DD9B98D43 P7464 "rigid-spine-muscular-dystrophy" @default.
- Q3025883-BADB8EBD-DA2F-4285-830C-9E7121624D36 P7464 "type-2-diabetes" @default.
- Q3026441-E388D4DA-049B-4D00-9722-272E633F2F99 P7464 "spinocerebellar-ataxia-type-3" @default.
- Q303123-FC95F719-1597-4BA3-9C49-E9E2B0ACC1AF P7464 "aarskog-scott-syndrome" @default.
- Q3042143-55678EAF-24E0-45A3-8BA5-847685C4ADA2 P7464 "frontometaphyseal-dysplasia" @default.
- Q3042171-C9CFA2BE-847E-4649-BC57-ED42AECBACFB P7464 "oculopharyngeal-muscular-dystrophy" @default.
- Q3043143-453F48C9-3848-4719-B3C3-12111D89A33A P7464 "carnitine-palmitoyltransferase-i-deficiency" @default.
- Q3043149-6FD4C3D2-D57A-4DEB-814F-E4F9633CC244 P7464 "pyruvate-kinase-deficiency" @default.
- Q3043153-F6057A1B-EC71-4614-9F78-1A7F81CED6BA P7464 "protein-s-deficiency" @default.
- Q3043155-048D693D-0AB2-47F0-AE04-39DAA5992F48 P7464 "purine-nucleoside-phosphorylase-deficiency" @default.
- Q3043158-CE11B32F-B2F1-4C05-AA3E-8010E9B1653C P7464 "mevalonate-kinase-deficiency" @default.
- Q3043161-95A4F0EF-268A-4518-98A3-FDEBAB147559 P7464 "ornithine-transcarbamylase-deficiency" @default.
- Q3045238-E4906E08-8140-48AA-9528-0B1B30C655DD P7464 "congenital-insensitivity-to-pain" @default.
- Q3053945-863C6F94-4FC7-4D6C-91FF-1190187EA1FC P7464 "glycine-encephalopathy" @default.
- Q30587718-1FC10F60-33F1-4DCD-BEE1-8DB71E1AC8D9 P7464 "sporadic-hemiplegic-migraine" @default.
- Q3071315-7A901E83-DC0F-4648-9E9A-2A8E699D5C0F P7464 "fibrochondrogenesis" @default.
- Q3085434-FFED052F-7EBF-4DCB-A7A4-55AA3AF7C19A P7464 "pallister-hall-syndrome" @default.
- Q309067-90AB2223-31F4-449D-9563-95F27CE56EC3 P7464 "motion-sickness" @default.
- Q30989658-DADA7A31-5854-4C3C-A449-8DE202EB834B P7464 "aromatic-l-amino-acid-decarboxylase-deficiency" @default.
- Q30989792-D69B0911-75B1-469F-AFB5-77DCFCFC6AFD P7464 "plcg2-associated-antibody-deficiency-and-immune-dysregulation" @default.
- Q30989948-29CA9867-33B8-4E68-A9A9-06D928755DD3 P7464 "autosomal-dominant-hypocalcemia" @default.
- Q310335-F342048C-7322-4C10-B650-8935FE1CD6CE P7464 "schindler-disease" @default.
- Q3124960-230FEBD4-B96D-45EE-9AD3-70AFAC6DFF7C P7464 "epidermolysis-bullosa-simplex" @default.
- Q3144217-4BBBFB5F-AAC1-443A-846C-D2D5D3F2E512 P7464 "myostatin-related-muscle-hypertrophy" @default.
- Q3144300-2869DE8B-D983-4982-802C-6EA6141F8494 P7464 "x-linked-adrenal-hypoplasia-congenita" @default.
- Q3153671-FFAE65B3-3A43-4594-BEED-21E8D9CEF62B P7464 "lysinuric-protein-intolerance" @default.
- Q31841284-26C8D2E0-5739-4E68-8718-773759C90622 P7464 "histiocytosis-lymphadenopathy-plus-syndrome" @default.
- Q319812-7D756180-2587-4D87-B7C4-788DC111DA8B P7464 "familial-hypobetalipoproteinemia" @default.
- Q319812-DDCE62FF-16CC-49CF-8F2B-A814CBC1A87B P7464 "abetalipoproteinemia" @default.
- Q32038811-E8D5AE2E-1A58-47DE-96B6-E30B8949289B P7464 "dystonia-16" @default.
- Q32038818-F491508E-70DB-4B31-A70D-C6A00389A921 P7464 "rapid-onset-dystonia-parkinsonism" @default.
- Q32137157-879D9571-17A3-411E-AC00-0C92062E8635 P7464 "thiopurine-s-methyltransferase-deficiency" @default.
- Q32140749-C66CD6BC-37FD-4DFE-8F9D-3C3CBD1123E1 P7464 "beta-propeller-protein-associated-neurodegeneration" @default.
- Q32142710-FA393366-EC4B-4642-BE61-576CAB931370 P7464 "spastic-paraplegia-type-2" @default.
- Q32146625-755B5A4B-9C5B-4A38-A674-9DBCB768F331 P7464 "glycoprotein-vi-deficiency" @default.
- Q32146709-89D930C2-D248-443F-AF43-D14E36E44FDB P7464 "hyperphosphatemic-familial-tumoral-calcinosis" @default.
- Q32146767-A514AC55-1EAC-469E-B7BC-D85571916990 P7464 "progressive-familial-heart-block" @default.
- Q3237080-F74FD48A-A298-40E1-83E2-9A2EE97034B1 P7464 "megalencephalic-leukoencephalopathy-with-subcortical-cysts" @default.
- Q3242224-26DA1FF5-9878-446B-92F4-59AB36C206C0 P7464 "congenital-generalized-lipodystrophy" @default.
- Q3269479-FCFCF175-AFFD-40DE-8D40-2E4C04BB62ED P7464 "familial-hemophagocytic-lymphohistiocytosis" @default.
- Q3269843-D88444AA-A16B-4D60-87C2-478AD53C67A4 P7464 "hyperkalemic-periodic-paralysis" @default.
- Q3270312-C532625C-9338-46A4-A5F6-BDFEF76BCC03 P7464 "hereditary-leiomyomatosis-and-renal-cell-cancer" @default.
- Q3278042-B64265B7-C94D-481D-9B80-2FBF72C1FB5C P7464 "isovaleric-acidemia" @default.
- Q3281227-50161B1C-8F62-4B94-9BC4-F573A6741FC9 P7464 "multiple-sulfatase-deficiency" @default.
- Q3281274-449493F8-6617-4BB3-926C-D189303A014D P7464 "griscelli-syndrome" @default.
- Q3281284-1FEF128B-08B2-4B2A-A409-4B153EF155BD P7464 "polycystic-lipomembranous-osteodysplasia-with-sclerosing-leukoencephalopathy" @default.
- Q3281380-508C88CA-722E-4A9A-82D7-61E6430CD57E P7464 "x-linked-lymphoproliferative-disease" @default.
- Q3281403-2ABDFF5B-B9D0-4326-8BE1-EB1D774BBEC9 P7464 "hepatic-veno-occlusive-disease-with-immunodeficiency" @default.
- Q3297103-E2F7FBF7-FC97-4A87-8D7E-30C7A07DE263 P7464 "1p36-deletion-syndrome" @default.
- Q3304152-9D8DDBC2-8CA2-459E-84D7-99047DA17D69 P7464 "jervell-and-lange-nielsen-syndrome" @default.
- Q3312899-F848E289-C530-4635-93B3-8071868874F7 P7464 "familial-hemiplegic-migraine" @default.
- Q332293-C5A9B303-BF33-4FEE-B7B0-14E4B739F72D P7464 "carpal-tunnel-syndrome" @default.
- Q3331454-97840517-D81F-4AEB-90C1-9F363571674C P7464 "x-linked-myotubular-myopathy" @default.
- Q3335660-0549811C-73AA-4076-BD00-8540F06ECB19 P7464 "3-m-syndrome" @default.
- Q3335666-B58A7EE6-9920-4605-B3A9-4828A78EFFC0 P7464 "diastrophic-dysplasia" @default.
- Q3338664-E16178DC-197E-457B-AF91-60F08163F858 P7464 "neuroferritinopathy" @default.
- Q3338682-090623C5-4D58-4515-B2D1-4BF444A159E4 P7464 "giant-axonal-neuropathy" @default.
- Q335555-515F6DD4-E174-464C-91CC-8F52365A6E18 P7464 "sjogren-syndrome" @default.
- Q3358135-DF246353-A7A5-4438-A546-1084AC0D62BE P7464 "primary-carnitine-deficiency" @default.
- Q3360152-D50213D7-62D5-4B52-BE98-44059D11B51A P7464 "pachyonychia-congenita" @default.
- Q3361967-A72A2B1F-5A20-4998-809F-D6451DC7F721 P7464 "hereditary-pancreatitis" @default.
- Q3363624-53A1A998-4FAF-45CB-A928-F83502720B49 P7464 "infantile-onset-ascending-hereditary-spastic-paralysis" @default.
- Q3363626-3AC52A44-639B-4EDE-A954-3F1EBBC8785B P7464 "spastic-paraplegia-type-7" @default.
- Q3368713-4C94B67D-0150-413E-8ACB-4303A44966C8 P7464 "leri-weill-dyschondrosteosis" @default.
- Q337604-B36DCE15-A3FD-426E-BC04-C3B0FB52C76A P7464 "aceruloplasminemia" @default.
- Q340594-282430B9-BB7B-4122-ACD2-FC055599D384 P7464 "achondroplasia" @default.
- Q341999-2D0F28DE-5446-43A5-88C9-7E41C7D9A8C1 P7464 "hidradenitis-suppurativa" @default.
- Q3501154-67D29D5D-EA8A-4092-8CCA-459FDF9CE168 P7464 "larsen-syndrome" @default.
- Q3508563-731FEBCF-F983-4752-9F95-EFCCD6B3AD1D P7464 "leukoencephalopathy-with-vanishing-white-matter" @default.
- Q3508566-B2C2E770-2F4B-4CCE-84F1-5CC0FEEE7910 P7464 "immune-dysregulation-polyendocrinopathy-enteropathy-x-linked-syndrome" @default.
- Q3508568-5E7BECE5-4781-4873-AED9-8213C7EC0038 P7464 "congenital-hemidysplasia-with-ichthyosiform-erythroderma-and-limb-defects" @default.