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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Spinocerebellar ataxia type 12
Idiopathic bronchiectasis

PPP2R2B CFTR
SCNN1A
SCNN1B
SCNN1G


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PPP2R2B
(0.63)
CFTR



Citations in the biomedical literature:


Spinocerebellar ataxia type 12
PPP2R2B
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Spinocerebellar ataxia type 12
Idiopathic bronchiectasis

Synonym(s):
- SCA12

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the respiratory system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.