Matches in Wikidata for { ?s <http://www.wikidata.org/prop/direct/P7464> ?o ?g. }
- Q2757585 P7464 "mowat-wilson-syndrome" @default.
- Q27677577 P7464 "megdel-syndrome" @default.
- Q27835675 P7464 "lmna-related-congenital-muscular-dystrophy" @default.
- Q28065590 P7464 "autosomal-dominant-leukodystrophy-with-autonomic-disease" @default.
- Q28065598 P7464 "hypomyelination-and-congenital-cataract" @default.
- Q28065629 P7464 "christianson-syndrome" @default.
- Q28065631 P7464 "ppm-x-syndrome" @default.
- Q281115 P7464 "proteus-syndrome" @default.
- Q28208917 P7464 "aminoacylase-1-deficiency" @default.
- Q2823145 P7464 "achondrogenesis" @default.
- Q2823332 P7464 "costeff-syndrome" @default.
- Q2823333 P7464 "succinic-semialdehyde-dehydrogenase-deficiency" @default.
- Q2823337 P7464 "fumarase-deficiency" @default.
- Q283108 P7464 "x-linked-agammaglobulinemia" @default.
- Q2831905 P7464 "ocular-albinism" @default.
- Q284219 P7464 "trisomy-13" @default.
- Q2852251 P7464 "abdominal-wall-defect" @default.
- Q2868786 P7464 "autosomal-recessive-spastic-ataxia-of-charlevoix-saguenay" @default.
- Q2868788 P7464 "spinocerebellar-ataxia-type-6" @default.
- Q2869820 P7464 "optic-atrophy-type-1" @default.
- Q2892779 P7464 "nephrogenic-diabetes-insipidus" @default.
- Q2894827 P7464 "childhood-absence-epilepsy" @default.
- Q29014971 P7464 "auriculo-condylar-syndrome" @default.
- Q291617 P7464 "beta-mannosidosis" @default.
- Q2936204 P7464 "hereditary-diffuse-gastric-cancer" @default.
- Q2966732 P7464 "ring-chromosome-14-syndrome" @default.
- Q2966733 P7464 "ring-chromosome-20-syndrome" @default.
- Q2991265 P7464 "polymicrogyria" @default.
- Q29982053 P7464 "otopalatodigital-syndrome-type-2" @default.
- Q29982088 P7464 "rigid-spine-muscular-dystrophy" @default.
- Q3025883 P7464 "type-2-diabetes" @default.
- Q3026441 P7464 "spinocerebellar-ataxia-type-3" @default.
- Q303123 P7464 "aarskog-scott-syndrome" @default.
- Q3042143 P7464 "frontometaphyseal-dysplasia" @default.
- Q3042171 P7464 "oculopharyngeal-muscular-dystrophy" @default.
- Q3043143 P7464 "carnitine-palmitoyltransferase-i-deficiency" @default.
- Q3043149 P7464 "pyruvate-kinase-deficiency" @default.
- Q3043153 P7464 "protein-s-deficiency" @default.
- Q3043155 P7464 "purine-nucleoside-phosphorylase-deficiency" @default.
- Q3043158 P7464 "mevalonate-kinase-deficiency" @default.
- Q3043161 P7464 "ornithine-transcarbamylase-deficiency" @default.
- Q3045238 P7464 "congenital-insensitivity-to-pain" @default.
- Q3053945 P7464 "glycine-encephalopathy" @default.
- Q30587718 P7464 "sporadic-hemiplegic-migraine" @default.
- Q3071315 P7464 "fibrochondrogenesis" @default.
- Q3085434 P7464 "pallister-hall-syndrome" @default.
- Q309067 P7464 "motion-sickness" @default.
- Q30989658 P7464 "aromatic-l-amino-acid-decarboxylase-deficiency" @default.
- Q30989792 P7464 "plcg2-associated-antibody-deficiency-and-immune-dysregulation" @default.
- Q30989948 P7464 "autosomal-dominant-hypocalcemia" @default.
- Q310335 P7464 "schindler-disease" @default.
- Q3124960 P7464 "epidermolysis-bullosa-simplex" @default.
- Q3144217 P7464 "myostatin-related-muscle-hypertrophy" @default.
- Q3144300 P7464 "x-linked-adrenal-hypoplasia-congenita" @default.
- Q3153671 P7464 "lysinuric-protein-intolerance" @default.
- Q31841284 P7464 "histiocytosis-lymphadenopathy-plus-syndrome" @default.
- Q319812 P7464 "abetalipoproteinemia" @default.
- Q319812 P7464 "familial-hypobetalipoproteinemia" @default.
- Q32038811 P7464 "dystonia-16" @default.
- Q32038818 P7464 "rapid-onset-dystonia-parkinsonism" @default.
- Q32137157 P7464 "thiopurine-s-methyltransferase-deficiency" @default.
- Q32140749 P7464 "beta-propeller-protein-associated-neurodegeneration" @default.
- Q32142710 P7464 "spastic-paraplegia-type-2" @default.
- Q32146625 P7464 "glycoprotein-vi-deficiency" @default.
- Q32146709 P7464 "hyperphosphatemic-familial-tumoral-calcinosis" @default.
- Q32146767 P7464 "progressive-familial-heart-block" @default.
- Q3237080 P7464 "megalencephalic-leukoencephalopathy-with-subcortical-cysts" @default.
- Q3242224 P7464 "congenital-generalized-lipodystrophy" @default.
- Q3269479 P7464 "familial-hemophagocytic-lymphohistiocytosis" @default.
- Q3269843 P7464 "hyperkalemic-periodic-paralysis" @default.
- Q3270312 P7464 "hereditary-leiomyomatosis-and-renal-cell-cancer" @default.
- Q3278042 P7464 "isovaleric-acidemia" @default.
- Q3281227 P7464 "multiple-sulfatase-deficiency" @default.
- Q3281274 P7464 "griscelli-syndrome" @default.
- Q3281284 P7464 "polycystic-lipomembranous-osteodysplasia-with-sclerosing-leukoencephalopathy" @default.
- Q3281380 P7464 "x-linked-lymphoproliferative-disease" @default.
- Q3281403 P7464 "hepatic-veno-occlusive-disease-with-immunodeficiency" @default.
- Q3297103 P7464 "1p36-deletion-syndrome" @default.
- Q3304152 P7464 "jervell-and-lange-nielsen-syndrome" @default.
- Q3312899 P7464 "familial-hemiplegic-migraine" @default.
- Q332293 P7464 "carpal-tunnel-syndrome" @default.
- Q3331454 P7464 "x-linked-myotubular-myopathy" @default.
- Q3335660 P7464 "3-m-syndrome" @default.
- Q3335666 P7464 "diastrophic-dysplasia" @default.
- Q3338664 P7464 "neuroferritinopathy" @default.
- Q3338682 P7464 "giant-axonal-neuropathy" @default.
- Q335555 P7464 "sjogren-syndrome" @default.
- Q3358135 P7464 "primary-carnitine-deficiency" @default.
- Q3360152 P7464 "pachyonychia-congenita" @default.
- Q3361967 P7464 "hereditary-pancreatitis" @default.
- Q3363624 P7464 "infantile-onset-ascending-hereditary-spastic-paralysis" @default.
- Q3363626 P7464 "spastic-paraplegia-type-7" @default.
- Q3368713 P7464 "leri-weill-dyschondrosteosis" @default.
- Q337604 P7464 "aceruloplasminemia" @default.
- Q340594 P7464 "achondroplasia" @default.
- Q341999 P7464 "hidradenitis-suppurativa" @default.
- Q3501154 P7464 "larsen-syndrome" @default.
- Q3508563 P7464 "leukoencephalopathy-with-vanishing-white-matter" @default.
- Q3508566 P7464 "immune-dysregulation-polyendocrinopathy-enteropathy-x-linked-syndrome" @default.
- Q3508568 P7464 "congenital-hemidysplasia-with-ichthyosiform-erythroderma-and-limb-defects" @default.