All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05733 HTX7 heterotaxy, visceral, autosomal, type 7 (HTX7) - AR - - MMP21 - -
06071 HTX7 Heterotaxy, visceral, 7, autosomal 616749 AR - - MMP21 - -
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