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Hereditary motor and sensory neuropathy type 6
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant Charcot-Marie-Tooth disease type 2A2
Autosomal dominant optic atrophy plus syndrome
Hereditary motor and sensory neuropathy type 5
Severe early-onset axonal neuropathy due to MFN2 deficiency
Young adult-onset Parkinsonism
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Intellectual deficit, X-linked, Turner type
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Synonym(s):
- CMT6
- Charcot-Marie-Tooth disease type 6
- Peripheral neuropathy and optic atrophy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MFN2 O95140608507
No signs/symptoms info available.