Deafness, Autosomal Recessive 21 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Recessive 21
Unique ID: C566353
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566353
Entry Term(s): DFNB21
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 2
Note: mutation in TECTA
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Recessive 21 Preferred

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