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
00602 - Spermatocytic seminoma, somatic 273300 - - - BCL10, FGFR3, KIT, STK11 - -
01427 - mast cell disease 154800 - - - KIT - -
00908 AML leukemia, myeloid, acute (AML) 601626 - - - CBFB, CEBPA, CHIC2, ETV6, FLT3, GATA2, JAK2, KIT, KRAS, LPP, MLF1, MLLT10, NPM1, NSD1, NUP214, PICALM, RUNX1, SH3GL1, TERT, WHSC1L1 - -
00468 FPH hyperpigmentation, progressive, familial (FPH) 145250 - - - KITLG - -
02601 GIST cancer, gastrointestinal stromal (GIST, gastrointestinal stromal tumor) 606764 - - - KIT, PDGFRA, SDHB, SDHC - -
01506 PBT Piebald trait (PBT) 172800 - - - KIT - -
00466 SHEP-7 pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation) 611664 - - - KITLG - -
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