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Autosomal dominant Charcot-Marie-Tooth disease type 2M
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

DNM2
(UniProt - OMIM)
 DNM2
(UniProt - OMIM)

COMMON
GENES 		DNM2


Citations in the biomedical literature:


Autosomal dominant Charcot-Marie-Tooth disease type 2M
DNM2
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B



Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

Synonym(s):
- CMT2M
Synonym(s):
- CMTDIB
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: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
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
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.