Deafness, Autosomal Recessive 1b MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Deafness, Autosomal Recessive 1b
Unique ID: C567213
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567213
Entry Term(s): DFNB1B
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Recessive 1b Preferred

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