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Deafness, Autosomal Recessive 31 MeSH Supplementary Concept Data 2023


MeSH Supplementary
Deafness, Autosomal Recessive 31
Unique ID
C564629
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564629
Entry Term(s)
DFNB31
Whirler, Mouse, Homolog Of
Registry Number
0
Heading Mapped to
*Hearing Loss, Sensorineural
Frequency
3
Note
mutation in WHRN
Date of Entry
2012/11/05
Deafness, Autosomal Recessive 31 Preferred
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