MeSH Browser

MeSH Supplementary: Amelogenesis Imperfecta, Type IB
Unique ID: C562879
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562879
Entry Term(s): Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant; Enamel Hypoplasia, Hereditary Localized
Registry Number: 0
Heading Mapped to: *Amelogenesis Imperfecta
Frequency: 1
Note: mutation in enamelin
Date of Entry: 2012/11/05

Amelogenesis Imperfecta, Type IB MeSH Supplementary Concept Data 2024