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Deafness, Autosomal Dominant 12 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Deafness, Autosomal Dominant 12
Unique ID
C563295
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563295
Entry Term(s)
DFNA12
DFNA8
Deafness, Autosomal Dominant 8
Registry Number
0
Heading Mapped to
*Hearing Loss, Sensorineural
Frequency
1
Note
mutation in TECTA gene
Date of Entry
2012/11/05
Deafness, Autosomal Dominant 12 Preferred
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