Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q55999785 P7464 "burn-mckeown-syndrome" @default.
- Q55999840 P7464 "proopiomelanocortin-deficiency" @default.
- Q56013758 P7464 "cap-myopathy" @default.
- Q56013902 P7464 "nakajo-nishimura-syndrome" @default.
- Q56013931 P7464 "l1-syndrome" @default.
- Q56013982 P7464 "hereditary-paraganglioma-pheochromocytoma" @default.
- Q56014009 P7464 "renal-tubular-dysgenesis" @default.
- Q56014213 P7464 "myosin-storage-myopathy" @default.
- Q56014268 P7464 "pseudohypoaldosteronism-type-2" @default.
- Q560337 P7464 "tay-sachs-disease" @default.
- Q5613758 P7464 "guanidinoacetate-methyltransferase-deficiency" @default.
- Q56694535 P7464 "cytochrome-p450-oxidoreductase-deficiency" @default.
- Q567820 P7464 "alexander-disease" @default.
- Q568865 P7464 "cherubism" @default.
- Q5714797 P7464 "hennekam-syndrome" @default.
- Q5737835 P7464 "adult-onset-leukoencephalopathy-with-axonal-spheroids-and-pigmented-glia" @default.
- Q580285 P7464 "mucopolysaccharidosis-type-iv" @default.
- Q580290 P7464 "spinal-muscular-atrophy" @default.
- Q582207 P7464 "antiphospholipid-syndrome" @default.
- Q587420 P7464 "myotonia-congenita" @default.
- Q5883885 P7464 "holocarboxylase-synthetase-deficiency" @default.
- Q594013 P7464 "prader-willi-syndrome" @default.
- Q5959327 P7464 "hypochondrogenesis" @default.
- Q5986449 P7464 "ichthyosis-with-confetti" @default.
- Q5996465 P7464 "irak-4-deficiency" @default.
- Q599683 P7464 "brugada-syndrome" @default.
- Q60195073 P7464 "intrahepatic-cholestasis-of-pregnancy" @default.
- Q60195313 P7464 "polycystic-kidney-disease" @default.
- Q6029060 P7464 "infantile-neuroaxonal-dystrophy" @default.
- Q60745615 P7464 "arginineglycine-amidinotransferase-deficiency" @default.
- Q609165 P7464 "juvenile-polyposis-syndrome" @default.
- Q610075 P7464 "wolf-hirschhorn-syndrome" @default.
- Q611458 P7464 "neuromyelitis-optica" @default.
- Q6118062 P7464 "jackson-weiss-syndrome" @default.
- Q611984 P7464 "keratoconus" @default.
- Q612108 P7464 "acute-promyelocytic-leukemia" @default.
- Q612693 P7464 "xeroderma-pigmentosum" @default.
- Q61335 P7464 "preeclampsia" @default.
- Q615645 P7464 "fabry-disease" @default.
- Q618246 P7464 "apert-syndrome" @default.
- Q61913473 P7464 "microcephaly-seizures-and-developmental-delay" @default.
- Q61913484 P7464 "early-infantile-epileptic-encephalopathy-1" @default.
- Q619428 P7464 "roberts-syndrome" @default.
- Q622437 P7464 "alpha-1-antitrypsin-deficiency" @default.
- Q622828 P7464 "hypokalemic-periodic-paralysis" @default.
- Q62736 P7464 "osteoarthritis" @default.
- Q630090 P7464 "glycogen-storage-disease-type-i" @default.
- Q6318969 P7464 "juvenile-primary-lateral-sclerosis" @default.
- Q633859 P7464 "poland-syndrome" @default.
- Q6378691 P7464 "kaufman-oculocerebrofacial-syndrome" @default.
- Q638975 P7464 "central-core-disease" @default.
- Q6422092 P7464 "kniest-dysplasia" @default.
- Q6491971 P7464 "laryngo-onycho-cutaneous-syndrome" @default.
- Q65066749 P7464 "alg1-congenital-disorder-of-glycosylation" @default.
- Q651680 P7464 "alkaptonuria" @default.
- Q6523439 P7464 "lenz-microphthalmia-syndrome" @default.
- Q6538005 P7464 "leydig-cell-hypoplasia" @default.
- Q6543864 P7464 "liebenberg-syndrome" @default.
- Q660330 P7464 "thrombocytopenia-absent-radius-syndrome" @default.
- Q66084696 P7464 "hypermanganesemia-with-dystonia" @default.
- Q669822 P7464 "laron-syndrome" @default.
- Q6737634 P7464 "majeed-syndrome" @default.
- Q6744526 P7464 "malonyl-coa-decarboxylase-deficiency" @default.
- Q6809999 P7464 "meige-disease" @default.
- Q6839323 P7464 "microcephalic-osteodysplastic-primordial-dwarfism-type-ii" @default.
- Q6839894 P7464 "microphthalmia-with-linear-skin-defects-syndrome" @default.
- Q6874652 P7464 "congenital-mirror-movement-disorder" @default.
- Q6881876 P7464 "mitochondrial-neurogastrointestinal-encephalopathy-disease" @default.
- Q6881883 P7464 "mitochondrial-trifunctional-protein-deficiency" @default.
- Q693519 P7464 "essential-tremor" @default.
- Q693578 P7464 "pseudoachondroplasia" @default.
- Q6951345 P7464 "n-acetylglutamate-synthase-deficiency" @default.
- Q709360 P7464 "von-willebrand-disease" @default.
- Q7103627 P7464 "ornithine-translocase-deficiency" @default.
- Q7104966 P7464 "orthostatic-hypotension" @default.
- Q7109017 P7464 "otospondylomegaepiphyseal-dysplasia" @default.
- Q7133011 P7464 "renal-coloboma-syndrome" @default.
- Q7138441 P7464 "parkes-weber-syndrome" @default.
- Q7139588 P7464 "paroxysmal-extreme-pain-disorder" @default.
- Q7202845 P7464 "platyspondylic-lethal-skeletal-dysplasia-torrance-type" @default.
- Q7234683 P7464 "potassium-aggravated-myotonia" @default.
- Q7234989 P7464 "potocki-shaffer-syndrome" @default.
- Q7243115 P7464 "primary-localized-cutaneous-amyloidosis" @default.
- Q7243137 P7464 "primary-hyperoxaluria" @default.
- Q724714 P7464 "romano-ward-syndrome" @default.
- Q7248854 P7464 "progressive-osseous-heteroplasia" @default.
- Q7249599 P7464 "prolidase-deficiency" @default.
- Q7250337 P7464 "propionic-acidemia" @default.
- Q7254411 P7464 "mucolipidosis-iii-alpha-beta" @default.
- Q7254644 P7464 "pseudocholinesterase-deficiency" @default.
- Q725845 P7464 "histidinemia" @default.
- Q7263591 P7464 "pyridoxine-dependent-epilepsy" @default.
- Q7263794 P7464 "pyruvate-carboxylase-deficiency" @default.
- Q7263801 P7464 "pyruvate-dehydrogenase-deficiency" @default.
- Q727436 P7464 "lesch-nyhan-syndrome" @default.
- Q729735 P7464 "chronic-myeloid-leukemia" @default.
- Q7320761 P7464 "rhizomelic-chondrodysplasia-punctata" @default.
- Q733493 P7464 "dandy-walker-malformation" @default.
- Q741315 P7464 "von-hippel-lindau-syndrome" @default.
- Q742500 P7464 "methylmalonic-acidemia" @default.