MeSH Browser

MeSH Supplementary: Amelogenesis Imperfecta, Type III
Unique ID: C562880
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562880
Entry Term(s): ADHCAI; Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant; Amelogenesis Imperfecta, Hypomineralization Type
Registry Numbers: 0
Heading Mapped to: *Amelogenesis Imperfecta
Frequency: 7
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Amelogenesis Imperfecta, Type III MeSH Supplementary Concept Data 2025