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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary motor and sensory neuropathy type 6
Autosomal dominant Charcot-Marie-Tooth disease type 2A2

MFN2 MFN2


COMMON
GENES
MFN2



Citations in the biomedical literature:


Hereditary motor and sensory neuropathy type 6
MFN2
Autosomal dominant Charcot-Marie-Tooth disease type 2A2



Hereditary motor and sensory neuropathy type 6
Autosomal dominant Charcot-Marie-Tooth disease type 2A2

Synonym(s):
- CMT6
- Charcot-Marie-Tooth disease type 6
- Peripheral neuropathy and optic atrophy

Synonym(s):
- CMT2A2

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.