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Deafness, Autosomal Dominant 48
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Deafness, Autosomal Dominant 48
Unique ID
C564322
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564322
Entry Term(s)
DFNA48
Registry Number
0
Heading Mapped to
*Hearing Loss, Sensorineural
Frequency
1
Note
mutation in MYO1A
Date of Entry
2012/11/05
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Deafness, Autosomal Dominant 48
Preferred
Concept UI
M0564622
Registry Number
0
Terms
Deafness, Autosomal Dominant 48
Preferred Term
Term UI
T804646
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
DFNA48
Term UI
T823523
Date
06/13/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
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