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
03478 CMH19 cardiomyopathy, hypertrophic, familial, type 19 (CMH-19) 613875 - - - CALR3 - -
01949 MMM myelofibrosis, with myeloid metaplasia, somatic 254450 - - - CALR, JAK2, MPL, SH2B3 - -
01578 THCYT1 thrombocythemia, type 1 187950 - 2 2 CALR, SH2B3, THPO - autosomal dominant
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