MeSH Browser

MeSH Supplementary: Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive
Unique ID: C564947
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564947
Entry Term(s): Charcot-Marie-Tooth Disease with Excessive Myelin Folding, Autosomal Recessive
Registry Number: 0
Heading Mapped to: *Hereditary Sensory and Motor Neuropathy
Frequency: 0
Date of Entry: 2012/11/05

Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive MeSH Supplementary Concept Data 2024