All diseases

13 entries on 1 page. Showing entries 1 - 13.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00683 - cancer, breast, familial 114480 - 8011 749 AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
00684 - SFM syndrome, somatic mosaic 163200 - 0 0 HRAS, KRAS, NRAS - -
00968 - Leukemia, acute myelogenous - - 0 0 KRAS - -
00639 ACLC cancer, lung (adenocarcinoma) 211980 - 11 8 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SLC22A18 - -
00908 AML leukemia, myeloid, acute (AML) 601626 - 43 28 CBFB, CEBPA, CHIC2, ETV6, FLT3, GATA2, JAK2, KIT, KRAS, LPP, MLF1, MLLT10, NPM1, NSD1, NUP214, PICALM, PTPN11, RUNX1, SH3GL1, TERT, WHSC1L1 - -
00315 cancer, bladder cancer, bladder 109800 - 60 60 FGFR3, HRAS, KRAS, RB1 - -
00681 cancer, pancreatic cancer, pancreatic 260350 - 34 24 KRAS, RBBP8, SMAD4, STK11, TP53 - -
00640 CFC-1 cardiofaciocutaneous syndrome, type 1 (CFC-1) 115150 - 2 2 BRAF, KRAS, MAP2K1, MAP2K2 - -
03880 CFC-2 cardiofaciocutaneous syndrome, type 2 (CFC-2) 615278 - 0 0 KRAS - -
00334 HDGC cancer, gastric, hereditary diffuse (HDGC) 137215 - 67 67 CDH1, IL1B, IL1RN, KRAS, MUTYH - -
00383 NS syndrome, Noonan (NS) - - 221 219 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2 - autosomal dominant
00682 NS-3 Noonan syndrome, type 3 (NS-3) 609942 - 3 3 KRAS - -
00555 RALD;ALPS-4 RAS-associated autoimmune leukoproliferative disorder (RALD, utoimmune lymphoproliferative syndrome type IV (ALPS-4)) 614470 - 3 3 KRAS, NRAS - -
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