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Deafness, Autosomal Recessive 21 MeSH Supplementary Concept Data 2025


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
2012/11/05
Deafness, Autosomal Recessive 21 Preferred
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