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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
Gardner syndrome
COG5-CDG

APC COG5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
COG5



Citations in the biomedical literature:


Gardner syndrome
APC
COG5-CDG
COG5



Gardner syndrome
COG5-CDG

Synonym(s):
(no synonyms)

Synonym(s):
- CDG syndrome type IIi
- CDG-IIi
- CDG2I
- Carbohydrate deficient glycoprotein syndrome type IIi
- Congenital disorder of glycosylation type IIi

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

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

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

External references:
1 OMIM reference -
1 MeSH reference: D005736
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.