All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03930 DUH3 dyschromatosis universalis hereditaria, type 3 (DUH-3) 615402 AD - - ABCB6 - -
01204 LAN blood group system, Langereis (LAN) 111600 - 1 1 ABCB6 - -
03670 MCOPCB7 microphthalmia, isolated, with coloboma, type 7 (MCOPCB-7) 614497 AD - - ABCB6 - -
06452 PSHK2 Pseudohyperkalemia, familial, 2, due to red cell leak 609153 AD - - ABCB6 - -
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