Amelogenesis Imperfecta, Type IB [Supplementary Concept]
mutation in enamelin
Date introduced: November 5, 2012
MeSH Unique ID: C562879
Heading Mapped to:
Entry Terms:
- Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant
- Enamel Hypoplasia, Hereditary Localized