MeSH Browser

MeSH Supplementary: Hereditary Motor And Sensory Neuropathy, Type IIC
Unique ID: C565261
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565261
Entry Term(s): CMT2C; Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C; Charcot-Marie-Tooth Neuropathy, Type 2C; HMSN IIC; HMSN2C
Registry Numbers: 0
Heading Mapped to: *Charcot-Marie-Tooth Disease
Frequency: 0
Note: mutation in TRPV4
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Concept UI: M0565561
Registry Numbers: 0
Terms: Hereditary Motor And Sensory Neuropathy, Type IIC Preferred Term
Term UI T823652
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013); Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C
Term UI T823651
Date06/14/2012
LexicalTag NON
ThesaurusID NLM (2013); HMSN2C
Term UI T823647
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013); Charcot-Marie-Tooth Neuropathy, Type 2C
Term UI T823650
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013); CMT2C
Term UI T823649
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013); HMSN IIC
Term UI T823648
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Hereditary Motor And Sensory Neuropathy, Type IIC MeSH Supplementary Concept Data 2025