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
05128 HTX heterotaxy, visceral (HTX, situs inversus/situs ambiguus) - - 102 100 C1orf127, PKD1L1 - -
06739 HTX8 Heterotaxy, visceral, 8, autosomal 617205 AR - - PKD1L1 - -
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