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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
COG4-CDG

APC COG4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
COG4



Citations in the biomedical literature:


APC-related attenuated familial adenomatous polyposis
APC
COG4-CDG
COG4



APC-related attenuated familial adenomatous polyposis
COG4-CDG

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

Synonym(s):
- CDG syndrome type IIj
- CDG-IIj
- CDG2J
- Carbohydrate deficient glycoprotein syndrome type IIj
- Congenital disorder of glycosylation type IIj

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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.