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Autosomal recessive centronuclear myopathy
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Autosomal dominant centronuclear myopathy
2 OMIM references -
4 associated genes
No signs/symptoms info
Autosomal recessive centronuclear myopathy
Autosomal dominant centronuclear myopathy

BIN1
(UniProt - OMIM)
 DNM2
(UniProt - OMIM)
TTN
(UniProt - OMIM)
 MTMR14
(UniProt - OMIM)
MYF6
(UniProt - OMIM)
RYR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TTN
BIN1
(0.63)
(0.52)
RYR1
DNM2


Citations in the biomedical literature:


Autosomal recessive centronuclear myopathy
BIN1 TTN
Autosomal dominant centronuclear myopathy
DNM2 MTMR14 MYF6 RYR1



Autosomal recessive centronuclear myopathy
Autosomal dominant centronuclear myopathy

Synonym(s):
- AR-CNM
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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
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.