MeSH Browser

MeSH Supplementary: Facial Hemihypertrophy
Unique ID: C563014
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563014
Entry Term(s): Hemifacial Hyperplasia
Heading Mapped to: Face / abnormalities; Facial Asymmetry / congenital; *Hyperplasia
Frequency: 65
Note: A congenital autosomal dominant abnormality characterized by asymmetry of the MANDIBLE, hypoplasia of the MAXILLA, and dental MALOCCLUSION. OMIM: 133900
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Facial Hemihypertrophy MeSH Supplementary Concept Data 2024