All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03416 HTX4 heterotaxy, visceral, autosomal, type 4 (HTX-4, situs ambiguus) 613751 - - - ACVR2B - -
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