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
00927 - cancer, colorectal, somatic - - 8 7 BRAF - -
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 - -
00640 CFC1 cardiofaciocutaneous syndrome, type 1 (CFC-1) 115150 AD 3 3 BRAF, KRAS, MAP2K1, MAP2K2 - -
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 - -
00642 LPRD3 LEOPARD syndrome, type 3 (LPRD-3) 613707 AD - - BRAF - -
00926 melanoma melanoma - - 393 172 BRAF, CDKN2A - -
00383 NS Noonan syndrome (NS) - - 232 225 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2, SPRED2 - autosomal dominant
00641 NS7 Noonan syndrome, type 7 (NS-7) 613706 AD 3 3 BRAF - -
00928 NSCLC cancer, lung, non-small cell (NSCLC) - - 13 11 BRAF - -
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