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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
4 associated genes
No signs/symptoms info
Machado-Joseph disease type 3
Autosomal dominant centronuclear myopathy

ATXN3 DNM2
MTMR14
MYF6
RYR1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATXN3
(0.63)
DNM2



Citations in the biomedical literature:


Machado-Joseph disease type 3
ATXN3
Autosomal dominant centronuclear myopathy
DNM2 MTMR14 MYF6 RYR1



Machado-Joseph disease type 3
Autosomal dominant centronuclear myopathy

Synonym(s):
- SCA3, Machado type

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: adulthood
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:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.