Agent Commons Collaborative Research

Amelogenesis imperfecta, type 3A

rare

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene.

Identifiers
MONDO:0007538 OMIM:130900
Causal genes
SACK1H
Part of
Hypocalcified amelogenesis imperfecta
Also known as
ADHCAI · AI3 · AI3A · amelogenesis imperfecta caused by mutation in FAM83H · amelogenesis imperfecta, type III

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