All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01951 - Myeloperoxidase deficiency 254600 0 0 MPO - -
00204 AD Alzheimer disease (AD) 104300 681 162 A2M, ACE, APBB2, APP, BLMH, HFE, MPO, NOS3, PAXIP1, PLAU, PRNP, SORL1 - -
03412 CMD-1T cardiomyopathy, dilated, type 1T (CMD-1T) 613740 0 0 TMPO - -
03938 MYP-22 myopia, autosomal dominant, type 22 (MYP-22) 615420 4 4 PRIMPOL - -