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Deafness, Autosomal Dominant, Due To Mutation In Myo1a
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Deafness, Autosomal Dominant, Due To Mutation In Myo1a
Unique ID
C567266
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567266
Heading Mapped to
Hearing Loss
/
congenital
Frequency
0
Date of Entry
2012/11/05
Revision Date
2013/11/06
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Deafness, Autosomal Dominant, Due To Mutation In Myo1a
Preferred
Concept UI
M0567566
Terms
Deafness, Autosomal Dominant, Due To Mutation In Myo1a
Preferred Term
Term UI
T810072
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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