Matches in Wikidata for { ?s <http://www.wikidata.org/prop/statement/P7464> ?o ?g. }
- Q55999785-92F5398D-FCE9-42B8-AA3D-2EB68392BE0B P7464 "burn-mckeown-syndrome" @default.
- Q55999840-51AEEFB6-7FAA-462E-A903-D0C793A44138 P7464 "proopiomelanocortin-deficiency" @default.
- Q56013758-9C1498F9-82FB-4B01-93B7-CE34BC9C7262 P7464 "cap-myopathy" @default.
- Q56013902-4316BB48-A80E-42B8-A04C-40F1AFDEEFEA P7464 "nakajo-nishimura-syndrome" @default.
- Q56013931-13B34220-8C80-41D5-BFEF-3E2BFA38577F P7464 "l1-syndrome" @default.
- Q56013982-F1AA2901-E2DB-4F07-94F7-7519843610EE P7464 "hereditary-paraganglioma-pheochromocytoma" @default.
- Q56014009-CE75DC35-29B9-4C29-B724-0338239E3BD1 P7464 "renal-tubular-dysgenesis" @default.
- Q56014213-806DA755-A361-4D6F-9FB1-FD9A0B037783 P7464 "myosin-storage-myopathy" @default.
- Q56014268-F90930D9-DBA1-46DC-9C5C-2740CBBE0C83 P7464 "pseudohypoaldosteronism-type-2" @default.
- Q560337-40AAB1B0-1C8D-4647-91AC-2A7702F4B86B P7464 "tay-sachs-disease" @default.
- Q5613758-BB85A5AC-4F59-4614-BE67-94FBCBED4BD3 P7464 "guanidinoacetate-methyltransferase-deficiency" @default.
- Q56694535-D1D8C1E5-B333-4B93-B81A-B0F718962656 P7464 "cytochrome-p450-oxidoreductase-deficiency" @default.
- Q567820-F8F03814-385D-4FD7-8634-F7DED820B809 P7464 "alexander-disease" @default.
- Q568865-ABC3449F-FF47-40E8-A78F-446854088BAF P7464 "cherubism" @default.
- Q5714797-987FAB11-9913-47EE-AAEA-700CFECD0394 P7464 "hennekam-syndrome" @default.
- Q5737835-9CE7AAB9-55A5-447C-B540-28E9EA6B2F0E P7464 "adult-onset-leukoencephalopathy-with-axonal-spheroids-and-pigmented-glia" @default.
- Q580285-F8814321-3693-4C1F-8652-3A23D9986B8D P7464 "mucopolysaccharidosis-type-iv" @default.
- Q580290-6796614C-CB5B-45C3-B4E2-781B9FDA0AF7 P7464 "spinal-muscular-atrophy" @default.
- Q582207-D5C1D493-15CE-46CE-BB92-A3E096C7729E P7464 "antiphospholipid-syndrome" @default.
- Q587420-6C02EAA3-31EC-4DDC-AA31-B8323C923924 P7464 "myotonia-congenita" @default.
- Q5883885-5DC56E1B-618F-44DE-B23F-CDE7FE4A085F P7464 "holocarboxylase-synthetase-deficiency" @default.
- Q594013-1A5C5F9E-763B-4AA4-8146-C7E27AE096AB P7464 "prader-willi-syndrome" @default.
- Q5959327-4B3424BC-9A06-4207-8ED4-7A5A07296246 P7464 "hypochondrogenesis" @default.
- Q5986449-BCA953C0-887F-4BE0-9EDB-D785E6D7178C P7464 "ichthyosis-with-confetti" @default.
- Q5996465-3D61D79C-CF52-4EA7-9F24-6221F0ACD845 P7464 "irak-4-deficiency" @default.
- Q599683-385B5CA4-1407-452D-8EF8-D688314BCE50 P7464 "brugada-syndrome" @default.
- Q60195073-61D7E774-4451-47A9-8C8E-459043240B78 P7464 "intrahepatic-cholestasis-of-pregnancy" @default.
- Q60195313-CBFE1F06-8EB9-4926-BD7A-BBF634E90CB0 P7464 "polycystic-kidney-disease" @default.
- Q6029060-D6A4F082-745D-460B-88B0-0E2EB5B025E2 P7464 "infantile-neuroaxonal-dystrophy" @default.
- Q60745615-D73F25C7-908A-476C-B352-3E15EA3C4775 P7464 "arginineglycine-amidinotransferase-deficiency" @default.
- Q609165-5C7E9E8C-707B-4AF5-8F47-401365915ED6 P7464 "juvenile-polyposis-syndrome" @default.
- Q610075-43CE8757-0ED7-4B5E-81FD-57DCF7A53E57 P7464 "wolf-hirschhorn-syndrome" @default.
- Q611458-9710720E-CD97-4DED-B44D-47C9BCE6C0FB P7464 "neuromyelitis-optica" @default.
- Q6118062-065114CC-D690-4939-9009-E99D1D505923 P7464 "jackson-weiss-syndrome" @default.
- Q611984-F6A4C448-DC9F-4199-9AE7-FF7AE06D5369 P7464 "keratoconus" @default.
- Q612108-9CB92708-380C-47F7-90D5-4F505FD46791 P7464 "acute-promyelocytic-leukemia" @default.
- Q612693-19FE732D-EA95-4304-B189-8C2F744E2C07 P7464 "xeroderma-pigmentosum" @default.
- Q61335-D8E4BDF1-04A7-42A3-9C43-704D5F125529 P7464 "preeclampsia" @default.
- Q615645-6FB956B4-07BC-4345-9AAB-EAAEA55EC067 P7464 "fabry-disease" @default.
- Q618246-F7C9658E-381E-489E-BA55-D00015F53D40 P7464 "apert-syndrome" @default.
- Q61913473-38D0B77A-D403-42BC-9E45-FF8751ED175F P7464 "microcephaly-seizures-and-developmental-delay" @default.
- Q61913484-BE37A9E4-880B-48E2-B36D-6AF7B240446A P7464 "early-infantile-epileptic-encephalopathy-1" @default.
- Q619428-F99460E3-729C-4571-B509-7CB5DCE84BB3 P7464 "roberts-syndrome" @default.
- Q622437-E7F45118-441B-4DD4-A75F-B6EE2CF49F6F P7464 "alpha-1-antitrypsin-deficiency" @default.
- Q622828-43883D35-A936-41C6-A23B-69C4941AE86F P7464 "hypokalemic-periodic-paralysis" @default.
- Q62736-0E3BDAE8-363D-4C83-A1FF-1415AA97046F P7464 "osteoarthritis" @default.
- Q630090-62A6A0C8-CEC7-42F7-AB6F-F786DE13FBFB P7464 "glycogen-storage-disease-type-i" @default.
- Q6318969-DC95D6FD-0F61-4CD2-8927-3373F2B1E79F P7464 "juvenile-primary-lateral-sclerosis" @default.
- Q633859-FBAA041A-3E3C-444A-98AE-21B99F4304B5 P7464 "poland-syndrome" @default.
- Q6378691-E1CD71A7-4D63-42C9-B425-FD07C2087A3A P7464 "kaufman-oculocerebrofacial-syndrome" @default.
- Q638975-F5D19F20-64B2-45AB-B147-113664EA657B P7464 "central-core-disease" @default.
- Q6422092-384988FA-1F53-4BC4-8173-4C74ACEA0201 P7464 "kniest-dysplasia" @default.
- Q6491971-85DD4558-0F29-4989-9413-0BB042B0CECD P7464 "laryngo-onycho-cutaneous-syndrome" @default.
- Q65066749-E69FA5FE-698F-4DE6-AF2A-CEB4FE1F94AA P7464 "alg1-congenital-disorder-of-glycosylation" @default.
- Q651680-BCD389CA-B980-4683-ABEC-7D949A2A11A4 P7464 "alkaptonuria" @default.
- Q6523439-54CE3DCF-78FB-44E3-88F8-CA14494516B3 P7464 "lenz-microphthalmia-syndrome" @default.
- Q6538005-4687E1B9-9D19-4650-8979-0A58DD49DA64 P7464 "leydig-cell-hypoplasia" @default.
- Q6543864-FCEC4EDD-91A1-4DE7-A1BE-CCFD51B90EF5 P7464 "liebenberg-syndrome" @default.
- Q660330-E43714AB-9EEE-4C86-AB06-10206B4055CE P7464 "thrombocytopenia-absent-radius-syndrome" @default.
- Q66084696-6FA45648-BAD2-4F40-88CF-4ABA8F22C242 P7464 "hypermanganesemia-with-dystonia" @default.
- Q669822-B2981C1A-012D-4BB3-8872-29E597C4EB5C P7464 "laron-syndrome" @default.
- Q6737634-22B0DA91-C5B4-4951-8074-62DDBFFA1EED P7464 "majeed-syndrome" @default.
- Q6744526-BB95E203-E23C-4F62-8FC1-A8D9A4ECD1F1 P7464 "malonyl-coa-decarboxylase-deficiency" @default.
- Q6809999-4E0131CD-C6AB-4FB9-8AB7-66406A260187 P7464 "meige-disease" @default.
- Q6839323-9D091097-DE18-4032-8EB0-A9AB3EE19337 P7464 "microcephalic-osteodysplastic-primordial-dwarfism-type-ii" @default.
- Q6839894-3E83CBD0-0B2C-46CD-B363-4B592B4A80B4 P7464 "microphthalmia-with-linear-skin-defects-syndrome" @default.
- Q6874652-F33503D0-9980-4FA5-955F-6020668A4610 P7464 "congenital-mirror-movement-disorder" @default.
- Q6881876-455A7005-EE5C-4A2D-8182-A25C04DA8B9A P7464 "mitochondrial-neurogastrointestinal-encephalopathy-disease" @default.
- Q6881883-6EDB16EB-1BB4-4830-88C1-35F233E1C6A6 P7464 "mitochondrial-trifunctional-protein-deficiency" @default.
- Q693519-E663DC8F-4F4E-439B-A8C9-A1CA519162E2 P7464 "essential-tremor" @default.
- Q693578-0758C771-8CC3-470A-A51C-3889BF7FD0A5 P7464 "pseudoachondroplasia" @default.
- Q6951345-BBF9E611-B442-4550-B4D4-1428092FE05F P7464 "n-acetylglutamate-synthase-deficiency" @default.
- Q709360-CE7C6BAD-7F19-40DD-A4B8-E29D38CBD947 P7464 "von-willebrand-disease" @default.
- Q7103627-5668B158-DE4E-49E8-AB38-9561F114DED1 P7464 "ornithine-translocase-deficiency" @default.
- Q7104966-F511B908-7511-4738-AC7D-203822546227 P7464 "orthostatic-hypotension" @default.
- Q7109017-8C0F56FC-0960-4141-A232-6919E0FE901C P7464 "otospondylomegaepiphyseal-dysplasia" @default.
- Q7133011-6E03FBC8-A916-4D13-AF83-DF89C9E0F268 P7464 "renal-coloboma-syndrome" @default.
- Q7138441-85BAAEE3-839F-426D-8F3C-D6BFBD07B091 P7464 "parkes-weber-syndrome" @default.
- Q7139588-3A004B5D-8DE7-4534-AF13-D253D55C90AF P7464 "paroxysmal-extreme-pain-disorder" @default.
- Q7202845-08582791-BB2C-4729-8698-C85C0FC8F40C P7464 "platyspondylic-lethal-skeletal-dysplasia-torrance-type" @default.
- Q7234683-C5070CC0-7738-4FFA-9FD6-28FF79131B1A P7464 "potassium-aggravated-myotonia" @default.
- Q7234989-39623225-9EB1-4365-96B5-A1DB7E525FAC P7464 "potocki-shaffer-syndrome" @default.
- Q7243115-62027F71-2B11-4956-B011-6269D9630A28 P7464 "primary-localized-cutaneous-amyloidosis" @default.
- Q7243137-41D127DE-F79E-48E8-AB19-A39A1658151F P7464 "primary-hyperoxaluria" @default.
- Q724714-D2B95A69-509F-4873-AFF6-944719995A81 P7464 "romano-ward-syndrome" @default.
- Q7248854-690A9073-506A-41EC-9998-66E3D7AD807B P7464 "progressive-osseous-heteroplasia" @default.
- Q7249599-450130A0-F1BE-4E02-8D1B-20746D53F239 P7464 "prolidase-deficiency" @default.
- Q7250337-6F22690B-AB4E-494D-B6D6-A234D4B242A0 P7464 "propionic-acidemia" @default.
- Q7254411-E2031A36-DFE7-482D-AB25-551FD4EED82F P7464 "mucolipidosis-iii-alpha-beta" @default.
- Q7254644-A96CD0E8-AD11-4AB3-8319-E88A0CD9B372 P7464 "pseudocholinesterase-deficiency" @default.
- Q725845-79444936-1146-4811-97C2-D3CFED598597 P7464 "histidinemia" @default.
- Q7263591-6799B5B4-5057-4424-B1B7-A3C056AE328F P7464 "pyridoxine-dependent-epilepsy" @default.
- Q7263794-E8B7B5A9-165C-473D-8540-2B1A4786450B P7464 "pyruvate-carboxylase-deficiency" @default.
- Q7263801-0373DDF2-8146-42AD-89C6-438CBEC9869C P7464 "pyruvate-dehydrogenase-deficiency" @default.
- Q727436-96DB9431-79E2-4221-ADD4-8570165635E5 P7464 "lesch-nyhan-syndrome" @default.
- Q729735-D591E716-7000-4C9A-A5BD-58845D9F4269 P7464 "chronic-myeloid-leukemia" @default.
- Q7320761-F700F4C8-5FF4-4EB4-BB45-14DA2606230B P7464 "rhizomelic-chondrodysplasia-punctata" @default.
- Q733493-540FB2E3-AC43-4CCF-917C-67A28D8CF649 P7464 "dandy-walker-malformation" @default.
- Q741315-E403FD65-E82E-4DE6-AFCF-51D02FDAD735 P7464 "von-hippel-lindau-syndrome" @default.
- Q742500-2B42D882-D880-41EB-9F7C-928884504CBB P7464 "methylmalonic-acidemia" @default.