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
01171 AI1B amelogenesis imperfecta, type IB (AI1B) 104500 AD - - ENAM - -
01650 AI1C amelogenesis imperfecta, type IC (AI1C) 204650 AR - - ENAM - -
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