All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00600 - nevus, epidermal 162900 - 1 1 FGFR3, HRAS, NRAS, PIK3CA - -
01343 CMNS nevus syndrome, melanocytic, congenital, somatic 137550 - - - HRAS, NRAS - -
00091 CRC cancer, colorectal, susceptibility to (CRC) 114500 AD;SMu 3065 1838 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) - - 2706 2388 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
01912 NCMS melanosis, neurocutaneous (NCMS) 249400 - - - NRAS - -
00554 NMTC2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 AD;SMu - - HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
00383 NS Noonan syndrome (NS) - - 232 225 BRAF, KRAS, LZTR1, NRAS, PTPN11, RAF1, RIT1, SOS1, SOS2, SPRED2 - autosomal dominant
00556 NS6 Noonan syndrome, type 6 (NS-6) 613224 AD 18 19 NRAS - -
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 - - - HRAS, KRAS, NRAS - -
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