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
00600 - nevus, epidermal 162900 - - - FGFR3, HRAS, NRAS, PIK3CA - -
00684 - SFM syndrome, somatic mosaic 163200 - - - HRAS, KRAS, NRAS - -
01343 - Giant pigmented hairy nevus 137550 - - - HRAS, NRAS - -
00091 CRC cancer, colorectal (CRC) 114500 - - - AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01912 NCMS melanosis, neurocutaneous (NCMS) 249400 - - - NRAS - -
00554 NMTC-2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 - - - HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
00556 NS-6 Noonan syndrome, type 6 (NS-6) 613224 - - - NRAS - -
00555 RALD;ALPS-4 RAS-associated autoimmune leukoproliferative disorder (RALD, utoimmune lymphoproliferative syndrome type IV (ALPS-4)) 614470 - - - KRAS, NRAS - -
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