Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q187255 P7464 "rheumatoid-arthritis" @default.
- Q187542 P7464 "li-fraumeni-syndrome" @default.
- Q1876206 P7464 "pelizaeus-merzbacher-disease" @default.
- Q187842 P7464 "hashimoto-thyroiditis" @default.
- Q1891209 P7464 "mycosis-fungoides" @default.
- Q1892153 P7464 "wagr-syndrome" @default.
- Q18932745 P7464 "autosomal-recessive-axonal-neuropathy-with-neuromyotonia" @default.
- Q189561 P7464 "narcolepsy" @default.
- Q18966102 P7464 "baraitser-winter-syndrome" @default.
- Q18966134 P7464 "rippling-muscle-disease" @default.
- Q190564 P7464 "huntington-disease" @default.
- Q1906054 P7464 "mucopolysaccharidosis-type-i" @default.
- Q1915681 P7464 "meckel-syndrome" @default.
- Q191779 P7464 "tourette-syndrome" @default.
- Q194041 P7464 "phenylketonuria" @default.
- Q1947298 P7464 "glycogen-storage-disease-type-vi" @default.
- Q1947307 P7464 "primary-familial-brain-calcification" @default.
- Q1951267 P7464 "moyamoya-disease" @default.
- Q1955377 P7464 "fukuyama-congenital-muscular-dystrophy" @default.
- Q1958739 P7464 "persistent-mullerian-duct-syndrome" @default.
- Q1965082 P7464 "essential-pentosuria" @default.
- Q1995327 P7464 "spinal-and-bulbar-muscular-atrophy" @default.
- Q1996246 P7464 "milroy-disease" @default.
- Q200985 P7464 "hartnup-disease" @default.
- Q2017218 P7464 "duane-radial-ray-syndrome" @default.
- Q2017741 P7464 "oculocutaneous-albinism" @default.
- Q201989 P7464 "lyme-disease" @default.
- Q2026857 P7464 "progressive-external-ophthalmoplegia" @default.
- Q202849 P7464 "turner-syndrome" @default.
- Q2033532 P7464 "van-der-woude-syndrome" @default.
- Q2033861 P7464 "carnitine-palmitoyltransferase-ii-deficiency" @default.
- Q2035074 P7464 "paget-disease-of-bone" @default.
- Q205214 P7464 "guillain-barre-syndrome" @default.
- Q206901 P7464 "amyotrophic-lateral-sclerosis" @default.
- Q207133 P7464 "klinefelter-syndrome" @default.
- Q208562 P7464 "marfan-syndrome" @default.
- Q209049 P7464 "1q211-microdeletion" @default.
- Q2096745 P7464 "hereditary-angioedema" @default.
- Q21097778 P7464 "spinocerebellar-ataxia-type-36" @default.
- Q21097855 P7464 "spinocerebellar-ataxia-type-1" @default.
- Q2110688 P7464 "tetrasomy-18p" @default.
- Q21113887 P7464 "familial-isolated-hyperparathyroidism" @default.
- Q21154055 P7464 "10q26-deletion-syndrome" @default.
- Q21154059 P7464 "15q24-microdeletion" @default.
- Q21154064 P7464 "17q12-deletion-syndrome" @default.
- Q2123641 P7464 "spondyloepimetaphyseal-dysplasia-strudwick-type" @default.
- Q2142496 P7464 "russell-silver-syndrome" @default.
- Q21503282 P7464 "episodic-ataxia" @default.
- Q21505516 P7464 "nonsyndromic-congenital-nail-disorder-10" @default.
- Q2160802 P7464 "congenital-nephrotic-syndrome" @default.
- Q2163245 P7464 "congenital-diaphragmatic-hernia" @default.
- Q2165663 P7464 "chronic-granulomatous-disease" @default.
- Q219223 P7464 "lactose-intolerance" @default.
- Q2200359 P7464 "mucopolysaccharidosis-type-iii" @default.
- Q2214419 P7464 "omenn-syndrome" @default.
- Q221472 P7464 "fragile-x-syndrome" @default.
- Q22443082 P7464 "spinocerebellar-ataxia-type-2" @default.
- Q22443772 P7464 "anonychia-congenita" @default.
- Q2272470 P7464 "carpenter-syndrome" @default.
- Q2288646 P7464 "stickler-syndrome" @default.
- Q2290446 P7464 "idiopathic-pulmonary-fibrosis" @default.
- Q2295338 P7464 "smith-magenis-syndrome" @default.
- Q22965506 P7464 "mandibulofacial-dysostosis-with-microcephaly" @default.
- Q2349546 P7464 "canavan-disease" @default.
- Q23542366 P7464 "warsaw-breakage-syndrome" @default.
- Q23542367 P7464 "mitochondrial-complex-i-deficiency" @default.
- Q2397009 P7464 "choroideremia" @default.
- Q2406697 P7464 "tetra-amelia-syndrome" @default.
- Q2411095 P7464 "char-syndrome" @default.
- Q245455 P7464 "5q-minus-syndrome" @default.
- Q2467739 P7464 "donohue-syndrome" @default.
- Q2470609 P7464 "wagner-syndrome" @default.
- Q24975519 P7464 "warfarin-resistance" @default.
- Q24975607 P7464 "mecp2-duplication-syndrome" @default.
- Q2500124 P7464 "lipoid-proteinosis" @default.
- Q250449 P7464 "alpha-mannosidosis" @default.
- Q25098828 P7464 "activated-pi3k-delta-syndrome" @default.
- Q25111656 P7464 "xia-gibbs-syndrome" @default.
- Q25324164 P7464 "north-american-indian-childhood-cirrhosis" @default.
- Q25324166 P7464 "isolated-congenital-asplenia" @default.
- Q25324661 P7464 "ataxia-pancytopenia-syndrome" @default.
- Q2532540 P7464 "birt-hogg-dube-syndrome" @default.
- Q25339349 P7464 "familial-hyperaldosteronism" @default.
- Q25381003 P7464 "x-linked-lissencephaly-with-abnormal-genitalia" @default.
- Q2605012 P7464 "kearns-sayre-syndrome" @default.
- Q2613277 P7464 "alpha-thalassemia-x-linked-intellectual-disability-syndrome" @default.
- Q2628677 P7464 "marinesco-sjogren-syndrome" @default.
- Q2632848 P7464 "alternating-hemiplegia-of-childhood" @default.
- Q265936 P7464 "kawasaki-disease" @default.
- Q2666433 P7464 "mitochondrial-encephalomyopathy-lactic-acidosis-and-stroke-like-episodes" @default.
- Q268667 P7464 "atopic-dermatitis" @default.
- Q2691713 P7464 "miller-syndrome" @default.
- Q2703116 P7464 "15q11-q13-duplication-syndrome" @default.
- Q27043982 P7464 "globozoospermia" @default.
- Q2711291 P7464 "familial-hypercholesterolemia" @default.
- Q27164415 P7464 "alpha-methylacyl-coa-racemase-deficiency" @default.
- Q27164424 P7464 "otulipenia" @default.
- Q271759 P7464 "porphyria" @default.
- Q2735907 P7464 "cutis-laxa" @default.
- Q2756703 P7464 "septo-optic-dysplasia" @default.