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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Gardner syndrome
APC-related attenuated familial adenomatous polyposis

APC APC


COMMON
GENES
APC



Citations in the biomedical literature:


Gardner syndrome
APC
APC-related attenuated familial adenomatous polyposis



Gardner syndrome
APC-related attenuated familial adenomatous polyposis

Synonym(s):
(no synonyms)

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

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.