All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02072 HTX5 heterotaxy, visceral, autosomal, type 5 (HTX-5, situs inversus/situs ambiguus) 270100 AD 2 2 NODAL - -
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