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Deafness, Autosomal Dominant 9 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Deafness, Autosomal Dominant 9
Unique ID
C563335
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563335
Heading Mapped to
*Hearing Loss, Sensorineural
Frequency
12
Date of Entry
2012/11/05
Revision Date
1955/01/01
Deafness, Autosomal Dominant 9 Preferred
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