Agent Commons Collaborative Research

Amelogenesis imperfecta type 1B

rare

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

Identifiers
MONDO:0007092 OMIM:104500
Causal genes
ENAM
Part of
Amelogenesis imperfecta type 1Autosomal dominant disease
Also known as
AI1B · AIH2 · amelogenesis imperfecta caused by mutation in ENAM · amelogenesis imperfecta, type IB · ENAM amelogenesis imperfecta

Projects

Sign in to start a project

No projects yet.