Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q3508576 P7464 "neuropathy-ataxia-and-retinitis-pigmentosa" @default.
- Q3508578 P7464 "rapadilino-syndrome" @default.
- Q3508595 P7464 "andermann-syndrome" @default.
- Q3508618 P7464 "congenital-contractural-arachnodactyly" @default.
- Q3508635 P7464 "fryns-syndrome" @default.
- Q3508649 P7464 "greig-cephalopolysyndactyly-syndrome" @default.
- Q3508679 P7464 "muenke-syndrome" @default.
- Q3508705 P7464 "timothy-syndrome" @default.
- Q3508706 P7464 "troyer-syndrome" @default.
- Q3508750 P7464 "opitz-g-bbb-syndrome" @default.
- Q3508764 P7464 "hand-foot-genital-syndrome" @default.
- Q3508768 P7464 "lymphedema-distichiasis-syndrome" @default.
- Q3508783 P7464 "oral-facial-digital-syndrome" @default.
- Q3508795 P7464 "trichorhinophalangeal-syndrome-type-ii" @default.
- Q3508800 P7464 "congenital-myasthenic-syndrome" @default.
- Q3512243 P7464 "tumor-necrosis-factor-receptor-associated-periodic-syndrome" @default.
- Q3539030 P7464 "trichothiodystrophy" @default.
- Q356410 P7464 "adermatoglyphia" @default.
- Q3567797 P7464 "white-sponge-nevus" @default.
- Q3589131 P7464 "dystrophic-epidermolysis-bullosa" @default.
- Q3589157 P7464 "autosomal-dominant-nocturnal-frontal-lobe-epilepsy" @default.
- Q3591493 P7464 "erythrokeratodermia-variabilis-et-progressiva" @default.
- Q3616632 P7464 "beta-thalassemia" @default.
- Q365589 P7464 "46xx-testicular-disorder-of-sex-development" @default.
- Q36956 P7464 "leprosy" @default.
- Q3702898 P7464 "familial-dysautonomia" @default.
- Q3709312 P7464 "dyskeratosis-congenita" @default.
- Q3710440 P7464 "myoclonus-dystonia" @default.
- Q3725646 P7464 "frontonasal-dysplasia" @default.
- Q3731836 P7464 "lamellar-ichthyosis" @default.
- Q3731836 P7464 "nonbullous-congenital-ichthyosiform-erythroderma" @default.
- Q374036 P7464 "langerhans-cell-histiocytosis" @default.
- Q379038 P7464 "adult-polyglucosan-body-disease" @default.
- Q3801491 P7464 "epidermolytic-hyperkeratosis" @default.
- Q3843790 P7464 "myh9-related-disorder" @default.
- Q3851644 P7464 "systemic-mastocytosis" @default.
- Q3857106 P7464 "primary-myelofibrosis" @default.
- Q3924862 P7464 "intestinal-pseudo-obstruction" @default.
- Q3961685 P7464 "rabson-mendenhall-syndrome" @default.
- Q39656409 P7464 "potocki-lupski-syndrome" @default.
- Q3972207 P7464 "steatocystoma-multiplex" @default.
- Q402575 P7464 "dihydrolipoamide-dehydrogenase-deficiency" @default.
- Q402575 P7464 "maple-syrup-urine-disease" @default.
- Q403453 P7464 "aicardi-goutieres-syndrome" @default.
- Q403463 P7464 "aicardi-syndrome" @default.
- Q4052543 P7464 "vldlr-associated-cerebellar-hypoplasia" @default.
- Q41112 P7464 "schizophrenia" @default.
- Q4127187 P7464 "congenital-stromal-corneal-dystrophy" @default.
- Q4162392 P7464 "meesmann-corneal-dystrophy" @default.
- Q41861 P7464 "hypertension" @default.
- Q4216194 P7464 "arterial-tortuosity-syndrome" @default.
- Q42844 P7464 "depression" @default.
- Q4293116 P7464 "microvillus-inclusion-disease" @default.
- Q432396 P7464 "achromatopsia" @default.
- Q432814 P7464 "alstrom-syndrome" @default.
- Q4348144 P7464 "weaver-syndrome" @default.
- Q4352832 P7464 "ochoa-syndrome" @default.
- Q4354267 P7464 "senior-loken-syndrome" @default.
- Q441077 P7464 "blau-syndrome" @default.
- Q4412533 P7464 "aspartylglucosaminuria" @default.
- Q4420136 P7464 "multicentric-osteolysis-nodulosis-and-arthropathy" @default.
- Q4553565 P7464 "koolen-de-vries-syndrome" @default.
- Q457737 P7464 "trisomy-18" @default.
- Q458099 P7464 "triosephosphate-isomerase-deficiency" @default.
- Q4596905 P7464 "short-branched-chain-acyl-coa-dehydrogenase-deficiency" @default.
- Q461854 P7464 "amelogenesis-imperfecta" @default.
- Q4636618 P7464 "3q29-microdeletion-syndrome" @default.
- Q4675304 P7464 "acrocallosal-syndrome" @default.
- Q4676182 P7464 "acromicric-dysplasia" @default.
- Q467635 P7464 "multiple-myeloma" @default.
- Q4682223 P7464 "adenine-phosphoribosyltransferase-deficiency" @default.
- Q4682317 P7464 "adenylosuccinate-lyase-deficiency" @default.
- Q4690019 P7464 "african-iron-overload" @default.
- Q474237 P7464 "distal-18q-deletion-syndrome" @default.
- Q475086 P7464 "desmoid-tumor" @default.
- Q47715 P7464 "down-syndrome" @default.
- Q47912 P7464 "lung-cancer" @default.
- Q4795506 P7464 "aromatase-deficiency" @default.
- Q4795508 P7464 "aromatase-excess-syndrome" @default.
- Q4807981 P7464 "asphyxiating-thoracic-dystrophy" @default.
- Q4821698 P7464 "spondylocostal-dysostosis" @default.
- Q4821698 P7464 "spondylothoracic-dysostosis" @default.
- Q48340195 P7464 "glutamate-formiminotransferase-deficiency" @default.
- Q4897218 P7464 "beta-ketothiolase-deficiency" @default.
- Q4904691 P7464 "bietti-crystalline-dystrophy" @default.
- Q4919794 P7464 "bjornstad-syndrome" @default.
- Q493103 P7464 "paramyotonia-congenita" @default.
- Q4943512 P7464 "boomerang-dysplasia" @default.
- Q494922 P7464 "glycogen-storage-disease-type-iii" @default.
- Q4973199 P7464 "brody-myopathy" @default.
- Q498487 P7464 "camurati-engelmann-disease" @default.
- Q4990874 P7464 "congenital-fibrosis-of-the-extraocular-muscles" @default.
- Q500695 P7464 "retinoblastoma" @default.
- Q500816 P7464 "polycystic-ovary-syndrome" @default.
- Q501694 P7464 "congenital-insensitivity-to-pain-with-anhidrosis" @default.
- Q5034093 P7464 "cantu-syndrome" @default.
- Q50349727 P7464 "hereditary-sensory-and-autonomic-neuropathy-type-ii" @default.
- Q50349805 P7464 "mitochondrial-complex-iii-deficiency" @default.
- Q50349837 P7464 "subcortical-band-heterotopia" @default.
- Q5037834 P7464 "carbamoyl-phosphate-synthetase-i-deficiency" @default.