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 ACLC cancer, lung (adenocarcinoma) 211980 - 11 8 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SLC22A18 - -
00640 CFC-1 cardiofaciocutaneous syndrome, type 1 (CFC-1) 115150 - 2 2 BRAF, KRAS, MAP2K1, MAP2K2 - -
00139 ID intellectual disability (ID) - - 1033 910 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 520 more - -
00642 LPRD-3 LEOPARD syndrome, type 3 (LPRD-3) 613707 - 0 0 BRAF - -
00926 melanoma melanoma - - 388 167 BRAF, CDKN2A - -
00383 NS syndrome, Noonan (NS) - - 221 219 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2 - autosomal dominant
00641 NS-7 Noonan syndrome, type 7 (NS-7) 613706 - 1 1 BRAF - -
00928 NSCLC cancer, lung, non-small cell (NSCLC) - - 11 11 BRAF - -
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