MeSH Browser

MeSH Supplementary: Otodental Dysplasia
Unique ID: C563482
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563482
Entry Term(s): Chromosome 11q13 Deletion Syndrome; Oculootodental Syndrome; Otodental Syndrome; Otodental Syndrome With Coloboma
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 11; *Coloboma; *Hearing Loss, Sensorineural; *Tooth Abnormalities; *Chromosome Disorders
Frequency: 6
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Otodental Dysplasia MeSH Supplementary Concept Data 2024