Hereditary Motor And Sensory Neuropathy VI [Supplementary Concept]

mutation in MFN2

Date introduced: November 5, 2012

MeSH Unique ID: C562851

Heading Mapped to:

• Hereditary Sensory and Motor Neuropathy

Entry Terms:

• Peripheral Neuropathy And Optic Atrophy
• HMSN VI
• HMSN6
• Charcot-Marie-Tooth Disease, Type 6
• CMT6