Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q5044061 P7464 "carnitine-acylcarnitine-translocase-deficiency" @default.
- Q504775 P7464 "bladder-cancer" @default.
- Q5064109 P7464 "coats-plus-syndrome" @default.
- Q506433 P7464 "trimethylaminuria" @default.
- Q5075435 P7464 "alopecia-areata" @default.
- Q50846110 P7464 "hsd10-disease" @default.
- Q510912 P7464 "triple-x-syndrome" @default.
- Q511097 P7464 "psoriatic-arthritis" @default.
- Q511372 P7464 "krabbe-disease" @default.
- Q5119339 P7464 "junctional-epidermolysis-bullosa" @default.
- Q512313 P7464 "androgen-insensitivity-syndrome" @default.
- Q5156399 P7464 "complement-component-2-deficiency" @default.
- Q5160407 P7464 "congenital-afibrinogenemia" @default.
- Q5160422 P7464 "congenital-dyserythropoietic-anemia" @default.
- Q5160437 P7464 "congenital-hyperinsulinism" @default.
- Q5198214 P7464 "cyclic-neutropenia" @default.
- Q5203306 P7464 "d-bifunctional-protein-deficiency" @default.
- Q521863 P7464 "beckwith-wiedemann-syndrome" @default.
- Q5220984 P7464 "danon-disease" @default.
- Q524353 P7464 "erythromelalgia" @default.
- Q525642 P7464 "22q112-deletion-syndrome" @default.
- Q5264836 P7464 "desmosterolosis" @default.
- Q5276448 P7464 "dihydropyrimidine-dehydrogenase-deficiency" @default.
- Q52849 P7464 "ankylosing-spondylitis" @default.
- Q529292 P7464 "anencephaly" @default.
- Q530142 P7464 "fg-syndrome" @default.
- Q531012 P7464 "congenital-hypothyroidism" @default.
- Q5340515 P7464 "systemic-scleroderma" @default.
- Q535364 P7464 "angelman-syndrome" @default.
- Q53660462 P7464 "lysosomal-acid-lipase-deficiency" @default.
- Q5369177 P7464 "emanuel-syndrome" @default.
- Q5375429 P7464 "ollier-disease" @default.
- Q53951449 P7464 "dopamine-transporter-deficiency-syndrome" @default.
- Q540571 P7464 "fibromyalgia" @default.
- Q541244 P7464 "hereditary-spherocytosis" @default.
- Q541852 P7464 "uncombable-hair-syndrome" @default.
- Q5432932 P7464 "familial-atrial-fibrillation" @default.
- Q5432935 P7464 "familial-encephalopathy-with-neuroserpin-inclusion-bodies" @default.
- Q5432936 P7464 "familial-exudative-vitreoretinopathy" @default.
- Q5432945 P7464 "familial-partial-lipodystrophy" @default.
- Q5432947 P7464 "familial-male-limited-precocious-puberty" @default.
- Q543517 P7464 "juvenile-myoclonic-epilepsy" @default.
- Q5441566 P7464 "feingold-syndrome" @default.
- Q5463847 P7464 "focal-dermal-hypoplasia" @default.
- Q548719 P7464 "aniridia" @default.
- Q548984 P7464 "dentinogenesis-imperfecta" @default.
- Q5493754 P7464 "frasier-syndrome" @default.
- Q5513688 P7464 "gm2-gangliosidosis-ab-variant" @default.
- Q5514398 P7464 "gracile-syndrome" @default.
- Q5532501 P7464 "generalized-pustular-psoriasis" @default.
- Q5533246 P7464 "genitopatellar-syndrome" @default.
- Q55345670 P7464 "autosomal-dominant-optic-atrophy-and-cataract" @default.
- Q55345810 P7464 "autosomal-recessive-cerebellar-ataxia-type-1" @default.
- Q55345816 P7464 "leukoencephalopathy-with-brainstem-and-spinal-cord-involvement-and-lactate-elevation" @default.
- Q55345866 P7464 "leukoencephalopathy-with-thalamus-and-brainstem-involvement-and-high-lactate" @default.
- Q55346074 P7464 "cln4-disease" @default.
- Q5556985 P7464 "ghosal-hematodiaphyseal-dysplasia" @default.
- Q5558484 P7464 "giant-congenital-melanocytic-nevus" @default.
- Q55603216 P7464 "adenosine-deaminase-2-deficiency" @default.
- Q5560415 P7464 "pulmonary-alveolar-microlithiasis" @default.
- Q5562120 P7464 "gillespie-syndrome" @default.
- Q5572341 P7464 "glucose-galactose-malabsorption" @default.
- Q5572606 P7464 "glycogen-storage-disease-type-0" @default.
- Q55780814 P7464 "fibronectin-glomerulopathy" @default.
- Q55781317 P7464 "osteoglophonic-dysplasia" @default.
- Q55781611 P7464 "weyers-acrofacial-dysostosis" @default.
- Q55781796 P7464 "renal-hypouricemia" @default.
- Q55781919 P7464 "gorlin-chaudhry-moss-syndrome" @default.
- Q55781959 P7464 "juvenile-paget-disease" @default.
- Q55782066 P7464 "manitoba-oculotrichoanal-syndrome" @default.
- Q55782334 P7464 "isolated-sulfite-oxidase-deficiency" @default.
- Q55782468 P7464 "phosphoribosylpyrophosphate-synthetase-superactivity" @default.
- Q55782879 P7464 "hyperferritinemia-cataract-syndrome" @default.
- Q55783319 P7464 "bosma-arhinia-microphthalmia-syndrome" @default.
- Q55783391 P7464 "au-kline-syndrome" @default.
- Q55783410 P7464 "tyrosine-hydroxylase-deficiency" @default.
- Q55783570 P7464 "capillary-malformation-arteriovenous-malformation-syndrome" @default.
- Q55783605 P7464 "sudden-infant-death-with-dysgenesis-of-the-testes-syndrome" @default.
- Q55783693 P7464 "7q1123-duplication-syndrome" @default.
- Q55783694 P7464 "acral-peeling-skin-syndrome" @default.
- Q55783762 P7464 "neutral-lipid-storage-disease-with-myopathy" @default.
- Q55783830 P7464 "early-onset-myopathy-with-fatal-cardiomyopathy" @default.
- Q55783879 P7464 "myd88-deficiency" @default.
- Q55783901 P7464 "prekallikrein-deficiency" @default.
- Q55784063 P7464 "hepatic-lipase-deficiency" @default.
- Q55784267 P7464 "retinal-arterial-macroaneurysm-with-supravalvular-pulmonic-stenosis" @default.
- Q55784418 P7464 "leptin-receptor-deficiency" @default.
- Q55784600 P7464 "hypomyelination-with-brainstem-and-spinal-cord-involvement-and-leg-spasticity" @default.
- Q55784774 P7464 "hereditary-fibrosing-poikiloderma-with-tendon-contractures-myopathy-and-pulmonary-fibrosis" @default.
- Q55784783 P7464 "carbonic-anhydrase-va-deficiency" @default.
- Q55784812 P7464 "sting-associated-vasculopathy-with-onset-in-infancy" @default.
- Q55784895 P7464 "chops-syndrome" @default.
- Q55785188 P7464 "yao-syndrome" @default.
- Q55787312 P7464 "sialidosis" @default.
- Q55788668 P7464 "lissencephaly-with-cerebellar-hypoplasia" @default.
- Q55789135 P7464 "idiopathic-inflammatory-myopathy" @default.
- Q55790472 P7464 "pseudoxanthoma-elasticum" @default.
- Q558077 P7464 "williams-syndrome" @default.
- Q5598273 P7464 "gray-platelet-syndrome" @default.
- Q55999489 P7464 "winchester-syndrome" @default.