All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00600 - nevus, epidermal 162900 0 0 FGFR3, HRAS, NRAS, PIK3CA - -
00684 - SFM syndrome, somatic mosaic 163200 0 0 HRAS, KRAS, NRAS - -
01343 - Giant pigmented hairy nevus 137550 0 0 HRAS, NRAS - -
00091 CRC cancer, colorectal (CRC) 114500 2931 1707 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
01912 NCMS melanosis, neurocutaneous (NCMS) 249400 0 0 NRAS - -
00554 NMTC-2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 0 0 HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
00383 NS syndrome, Noonan (NS) - 221 219 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2 - autosomal dominant
00556 NS-6 Noonan syndrome, type 6 (NS-6) 613224 18 19 NRAS - -
00555 RALD;ALPS-4 RAS-associated autoimmune leukoproliferative disorder (RALD, utoimmune lymphoproliferative syndrome type IV (ALPS-4)) 614470 3 3 KRAS, NRAS - -