MeSH Browser

MeSH Supplementary: Deafness oligodontia syndrome
Unique ID: C538049
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538049
Entry Term(s): Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia; Congenital profound sensorineural deafness and oligodontia; Deafness-Oligodontia Syndrome
Registry Numbers: 0
Heading Mapped to: *Anodontia; *Hearing Loss, Sensorineural
Frequency: 1
Note: Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia
Date of Entry: 2010/08/25
Revision Date: 2012/12/01

Deafness oligodontia syndrome MeSH Supplementary Concept Data 2025