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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Spinocerebellar ataxia type 12

HSPD1 PPP2R2B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.56)
PPP2R2B



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Spinocerebellar ataxia type 12
PPP2R2B



Autosomal dominant spastic paraplegia type 13
Spinocerebellar ataxia type 12

Synonym(s):
- SPG13

Synonym(s):
- SCA12

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: <1 / 1 000 000
Average age onset: -
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:
1 OMIM reference -
1 MeSH reference: C537485
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.