MeSH Browser

MeSH Supplementary: Neuropathy, hereditary motor and sensory, LOM type
Unique ID: C535716
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535716
Entry Term(s): CMT4D; Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4d; Charcot-Marie-Tooth Disease, Type 4D; Charcot-Marie-Tooth Neuropathy, Type 4d; HMSN4D; HMSNL; Hereditary motor and sensory neuropathy, LOM type
Registry Numbers: 0
Heading Mapped to: *Charcot-Marie-Tooth Disease; *Refsum Disease
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Neuropathy, hereditary motor and sensory, LOM type MeSH Supplementary Concept Data 2025