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


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)
Registry Number
0
Heading Mapped to
*Laminopathies
*Charcot-Marie-Tooth Disease
Frequency
18
Date of Entry
2010/08/25
Revision Date
2020/02/28
Charcot-Marie-Tooth disease, Type 2B Preferred
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