MeSH Browser

MeSH Supplementary: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Unique ID: C565316
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565316
Entry Term(s): DFNA39-Dentinogenesis Imperfecta 1 Syndrome
Registry Numbers: 0
Heading Mapped to: *Dentinogenesis Imperfecta; *Hearing Loss, Sensorineural
Frequency: 0
Note: mutation in DSPP
Date of Entry: 2012/11/05
Revision Date: 2015/11/10

Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 MeSH Supplementary Concept Data 2025