MeSH Browser

MeSH Supplementary: Deafness, Autosomal Dominant 1
Unique ID: C565121
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565121
Entry Term(s): Deafness, Progressive Low Tone; Hereditary Low Frequency Hearing Loss; Konigsmark Syndrome
Registry Number: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 3
Date of Entry: 2012/11/05

Concept UI: M0565421
Registry Number: 0
Terms: Deafness, Autosomal Dominant 1 Preferred Term
Term UI T806192
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Konigsmark Syndrome
Term UI T806197
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hereditary Low Frequency Hearing Loss
Term UI T806196
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Deafness, Progressive Low Tone
Term UI T806193
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Deafness, Autosomal Dominant 1 MeSH Supplementary Concept Data 2023