Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Machado-Joseph disease type 3
Autosomal dominant Charcot-Marie-Tooth disease type 2M

ATXN3 DNM2


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 Charcot-Marie-Tooth disease type 2M
DNM2



Machado-Joseph disease type 3
Autosomal dominant Charcot-Marie-Tooth disease type 2M

Synonym(s):
- SCA3, Machado type

Synonym(s):
- CMT2M

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: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.