All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01578 - Essential thrombocythemia 187950 - - - CALR, SH2B3, THPO - -
01949 - Myelofibrosis 254450 - - - CALR, JAK2, MPL, SH2B3 - -
03478 CMH-19 cardiomyopathy, hypertrophic, familial, type 19 (CMH-19) 613875 - - - CALR3 - -
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