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 - 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 - -
00315 cancer, bladder cancer, bladder 109800 - 61 61 FGFR3, HRAS, KRAS, RB1 - -
01725 CSTLO Costello syndrome (CSTLO) 218040 - 3 3 HRAS - -
00139 ID intellectual disability (ID) - - 1837 1570 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
00554 NMTC-2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 - 0 0 HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
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