MeSH Browser

MeSH Supplementary: Hereditary Motor And Sensory Neuropathy VI
Unique ID: C562851
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562851
Entry Term(s): CMT6; Charcot-Marie-Tooth Disease, Type 6; HMSN VI; HMSN6; Peripheral Neuropathy And Optic Atrophy
Heading Mapped to: *Hereditary Sensory and Motor Neuropathy
Frequency: 1
Note: mutation in MFN2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Concept UI: M0563151
Terms: Hereditary Motor And Sensory Neuropathy VI Preferred Term
Term UI T824170
Date06/19/2012
LexicalTag NON
ThesaurusID OMIM (2013); Charcot-Marie-Tooth Disease, Type 6
Term UI T801652
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); CMT6
Term UI T824169
Date06/19/2012
LexicalTag NON
ThesaurusID OMIM (2013); HMSN VI
Term UI T824167
Date06/19/2012
LexicalTag NON
ThesaurusID OMIM (2013); HMSN6
Term UI T824168
Date06/19/2012
LexicalTag NON
ThesaurusID OMIM (2013); Peripheral Neuropathy And Optic Atrophy
Term UI T801655
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Hereditary Motor And Sensory Neuropathy VI MeSH Supplementary Concept Data 2025