All diseases

9 entries on 1 page. Showing entries 1 - 9.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00639 cancer, lung cancer, lung (adenocarcinoma) 211980 - 55 43 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SFTPA2, SLC22A18 - -
00855 CRPT2 Carpenter syndrome, type 2 (CRPT-2) 614976 AR - - MEGF8 - -
03629 EMARDD myopathy, areflexia, respiratory distress, and dysphagia, early-onset 614399 AR - 1 MEGF10 - -
03047 HOMG4 hypomagnesemia, type 4, renal (HOMG-4) 611718 - - - EGF - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
05327 LMPH lymphedema (LMPH) - IC 11 11 VEGFC - -
04128 LMPHM4 lymphatic malformation 4 615907 AD - - VEGFC - -
02475 MVCD1 microvascular complications of diabetes 1 (MVCD-1) 603933 - - - VEGFA - -
04460 NISBD2 inflammatory skin and bowel disease, neonatal, type 2 (NISBD-2) 616069 AR - - EGFR - -
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