MeSH Browser

MeSH Supplementary: Charcot-Marie-Tooth disease, Type 2B
Unique ID: C537989
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537989
Entry Term(s): CMT 2B; CMT2B; Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2B; Charcot-Marie-Tooth Neuropathy, Type 2B; Charcot-Marie-Tooth disease, axonal, Type 2B; Charcot-Marie-Tooth disease, neuronal, Type 2B; HMSN IIB; HMSN2B; Hereditary Motor And Sensory Neuropathy IIB; Hereditary motor and sensory neuropathy 2 B (HMSN 2 B); Peripheral sensory neuropathy, autosomal dominant (PSN)
Heading Mapped to: *Charcot-Marie-Tooth Disease; *Laminopathies
Frequency: 18
Date of Entry: 2010/08/25
Revision Date: 2020/02/28

Charcot-Marie-Tooth disease, Type 2B MeSH Supplementary Concept Data 2024