All diseases

16 entries on 1 page. Showing entries 1 - 16.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00968 - Leukemia, acute myelogenous - - 0 0 KRAS - -
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 - -
01183 BAVM arteriovenous malformation, cerebral, brain (BAVM 108010 - 2 2 IL6, KRAS - -
00315 cancer, bladder cancer, bladder 109800 - 61 61 FGFR3, HRAS, KRAS, RB1 - -
00683 cancer, breast cancer, breast, susceptibility 114480 - 8102 785 AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
00639 cancer, lung cancer, lung (adenocarcinoma) 211980 - 52 40 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SFTPA2, SLC22A18 - -
00681 cancer, pancreatic cancer, pancreatic 260350 - 63 51 KRAS, RBBP8, SMAD4, STK11, TP53 - -
00640 CFC1 cardiofaciocutaneous syndrome, type 1 (CFC-1) 115150 AD 2 2 BRAF, KRAS, MAP2K1, MAP2K2 - -
03880 CFC2 cardiofaciocutaneous syndrome, type 2 (CFC-2) 615278 AD 0 0 KRAS - -
00334 HDGC cancer, gastric, hereditary diffuse (HDGC) 137215 AD 69 69 CDH1, IL1B, IL1RN, KRAS, MUTYH - -
00139 ID intellectual disability (ID) - - 2195 1894 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 540 more - -
00383 NS Noonan syndrome (NS) - - 231 224 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2 - autosomal dominant
00682 NS3 Noonan syndrome, type 3 (NS-3) 609942 AD 3 3 KRAS - -
06161 OES Oculoectodermal syndrome, somatic 600268 - 0 0 KRAS - -
00555 RALD;ALPS4 RAS-associated autoimmune leukoproliferative disorder (RALD, utoimmune lymphoproliferative syndrome type IV (ALPS-4)) 614470 AD 3 3 KRAS, NRAS - -
00684 SFM Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic 163200 - 0 0 HRAS, KRAS, NRAS - -
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