MeSH Browser

MeSH Supplementary: Hagemoser Weinstein Bresnick syndrome
Unique ID: C537626
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537626
Entry Term(s): Optic atrophy, deafness and peripheral neuropathy; Optic atrophy, hearing loss and peripheral neuropathy
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Bilateral; *Hereditary Sensory and Motor Neuropathy; *Optic Atrophies, Hereditary
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Hagemoser Weinstein Bresnick syndrome MeSH Supplementary Concept Data 2025