MeSH Browser

MeSH Supplementary: Optic atrophy polyneuropathy deafness
Unique ID: C537129
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537129
Entry Term(s): Charcot-Marie-Tooth Disease, X-Linked Recessive, 5; Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 5; Familial opticoacoustic nerve degeneration and polyneuropathy; Optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive; Optic atrophy, neural deafness, and distal neurogenic amyotrophy; Optic atrophy, polyneuropathy, and deafness; Optic atrophy, sensorineural hearing loss and polyneuropathy; Rosenberg Chutorian syndrome; Rosenberg-Chutorian Syndrome
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Central; *Polyneuropathies; *Optic Atrophies, Hereditary; *Muscular Disorders, Atrophic
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2012/11/30

Optic atrophy polyneuropathy deafness MeSH Supplementary Concept Data 2024