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
06233 AI2A6 Amelogenesis imperfecta, hypomaturation type, IIA6 617217 AR - - GPR68 - -
06850 CBAVDX Congenital bilateral absence of vas deferens, X-linked 300985 XL - - GPR64 - -
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