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
00905 CCF clubfoot, congenital, with/without deficiency of long bones and/or mirror-image polydactyly (CCF) 119800 AD - - PITX1 - autosomal dominant
00906 LBNBG Liebenberg syndrome 186550 AD - - PITX1 - -
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