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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
APC-related attenuated familial adenomatous polyposis
Spectrin-associated autosomal recessive cerebellar ataxia

APC SPTBN2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
SPTBN2



Citations in the biomedical literature:


APC-related attenuated familial adenomatous polyposis
APC
Spectrin-associated autosomal recessive cerebellar ataxia
SPTBN2



APC-related attenuated familial adenomatous polyposis
Spectrin-associated autosomal recessive cerebellar ataxia

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli

Synonym(s):
- Autosomal recessive cerebellar ataxia - cognitive defect
- Autosomal recessive spinocerebellar ataxia type 14
- SCAR14
- SPARCA
- SPARCA1
- Spectrin-associated autosomal recessive cerebellar ataxia type 1

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
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: <1 / 1 000 000
Average age onset: neonatal/infancy
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.