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

DNM2
(UniProt - OMIM)
 DNM2
(UniProt - OMIM)
MTMR14
(UniProt - OMIM)
MYF6
(UniProt - OMIM)
RYR1
(UniProt - OMIM)

COMMON
GENES 		DNM2


Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2
Autosomal dominant centronuclear myopathy
MTMR14 MYF6 RYR1



Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant centronuclear myopathy

Synonym(s):
- CMTDIB
Synonym(s):
- AD-CNM
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: unknown
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.