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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive centronuclear myopathy

DNM2 BIN1
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DNM2
(0.52)
BIN1



Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2
Autosomal recessive centronuclear myopathy
BIN1 TTN



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

Synonym(s):
- CMTDIB

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

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

No signs/symptoms info available.