All diseases

7 entries on 1 page. Showing entries 1 - 7.
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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 - -
00315 cancer, bladder cancer, bladder 109800 - 63 63 FGFR3, HRAS, KRAS, RB1 - -
01343 CMNS nevus syndrome, melanocytic, congenital, somatic 137550 - - - HRAS, NRAS - -
01725 CSTLO Costello syndrome (CSTLO, myopathy with excess of muscle spindles ) 218040 AD 5 5 HRAS - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00554 NMTC2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 AD;SMu - - HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
00684 SFM Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic 163200 - - - HRAS, KRAS, NRAS - -
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