Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q744790 P7464 "treacher-collins-syndrome" @default.
- Q749409 P7464 "osteogenesis-imperfecta" @default.
- Q7506696 P7464 "sialic-acid-storage-disease" @default.
- Q7506696 P7464 "sialuria" @default.
- Q756289 P7464 "wilms-tumor" @default.
- Q7577467 P7464 "spinal-muscular-atrophy-with-lower-extremity-predominance" @default.
- Q7577468 P7464 "spinal-muscular-atrophy-with-progressive-myoclonic-epilepsy" @default.
- Q7578959 P7464 "spondyloperipheral-dysplasia" @default.
- Q7578960 P7464 "spondyloepiphyseal-dysplasia-congenita" @default.
- Q762713 P7464 "hypercholesterolemia" @default.
- Q7632698 P7464 "succinyl-coa3-ketoacid-coa-transferase-deficiency" @default.
- Q7706537 P7464 "tetrahydrobiopterin-deficiency" @default.
- Q773118 P7464 "andersen-tawil-syndrome" @default.
- Q774483 P7464 "galactosemia" @default.
- Q776026 P7464 "biotinidase-deficiency" @default.
- Q776881 P7464 "hereditary-hemorrhagic-telangiectasia" @default.
- Q779250 P7464 "crouzon-syndrome" @default.
- Q7801152 P7464 "tietz-syndrome" @default.
- Q781618 P7464 "cleidocranial-dysplasia" @default.
- Q782958 P7464 "centronuclear-myopathy" @default.
- Q7840696 P7464 "trichohepatoenteric-syndrome" @default.
- Q7876086 P7464 "uv-sensitive-syndrome" @default.
- Q787751 P7464 "glycogen-storage-disease-type-v" @default.
- Q790971 P7464 "bartter-syndrome" @default.
- Q7925271 P7464 "vici-syndrome" @default.
- Q7939442 P7464 "vohwinkel-syndrome" @default.
- Q8046191 P7464 "y-chromosome-infertility" @default.
- Q8277 P7464 "multiple-sclerosis" @default.
- Q8285 P7464 "myasthenia-gravis" @default.
- Q829150 P7464 "glycogen-storage-disease-type-iv" @default.
- Q830265 P7464 "vitelliform-macular-dystrophy" @default.
- Q830308 P7464 "age-related-macular-degeneration" @default.
- Q831530 P7464 "rosacea" @default.
- Q834047 P7464 "schizoaffective-disorder" @default.
- Q844717 P7464 "spina-bifida" @default.
- Q845779 P7464 "fanconi-anemia" @default.
- Q847057 P7464 "retinitis-pigmentosa" @default.
- Q848343 P7464 "glucose-6-phosphate-dehydrogenase-deficiency" @default.
- Q852574 P7464 "bunion" @default.
- Q858426 P7464 "5-alpha-reductase-deficiency" @default.
- Q859142 P7464 "citrullinemia" @default.
- Q861224 P7464 "juvenile-idiopathic-arthritis" @default.
- Q861645 P7464 "gaucher-disease" @default.
- Q884590 P7464 "incontinentia-pigmenti" @default.
- Q890470 P7464 "legius-syndrome" @default.
- Q914389 P7464 "cockayne-syndrome" @default.
- Q916280 P7464 "restless-legs-syndrome" @default.
- Q917227 P7464 "sandhoff-disease" @default.
- Q917357 P7464 "rett-syndrome" @default.
- Q917399 P7464 "usher-syndrome" @default.
- Q9182808 P7464 "stuve-wiedemann-syndrome" @default.
- Q9190339 P7464 "17q12-duplication" @default.
- Q928424 P7464 "barth-syndrome" @default.
- Q928767 P7464 "multiple-familial-trichoepithelioma" @default.
- Q931538 P7464 "mucolipidosis-type-iv" @default.
- Q9366868 P7464 "generalized-arterial-calcification-of-infancy" @default.
- Q938205 P7464 "neuroblastoma" @default.
- Q9390211 P7464 "branchio-oculo-facial-syndrome" @default.
- Q9390284 P7464 "netherton-syndrome" @default.
- Q9390545 P7464 "hyperparathyroidism-jaw-tumor-syndrome" @default.
- Q940210 P7464 "ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome" @default.
- Q945930 P7464 "progressive-supranuclear-palsy" @default.
- Q948318 P7464 "polycythemia-vera" @default.
- Q953638 P7464 "wiskott-aldrich-syndrome" @default.
- Q959211 P7464 "chylomicron-retention-disease" @default.
- Q97610297 P7464 "syngap1-related-intellectual-disability" @default.
- Q994859 P7464 "homocystinuria" @default.