All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01949 - Myelofibrosis 254450 - - - CALR, JAK2, MPL, SH2B3 - -
02406 - Thrombocytosis, benign familial microcytic 601977 - - - MPL - -
02514 CAMT thrombocytopenia, amegakaryocytic, congenital (CAMT) 604498 - - - MPL - -
00748 TTD trichothiodystrophy (TTD) - - - - ERCC2, ERCC3, GTF2H5, MPLKIP - -
01835 TTD-4;TTDN-1 trichothiodystrophy, type 4, nonphotosensitive (TTD-4, TTDN-1) 234050 - - - MPLKIP - -
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