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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 associated gene
No signs/symptoms info
Gardner syndrome
Familial adenomatous polyposis due to 5q22.2 microdeletion

APC APC


COMMON
GENES
APC



Citations in the biomedical literature:


Gardner syndrome
APC
Familial adenomatous polyposis due to 5q22.2 microdeletion



Gardner syndrome
Familial adenomatous polyposis due to 5q22.2 microdeletion

Synonym(s):
(no synonyms)

Synonym(s):
- Colorectal adenomatous polyposis due to monosomy 5q22.2
- FAP due to monosomy 5q22.2
- Familial adenomatous polyposis due to del(5)(q22.2)
- Familial adenomatous polyposis due to monosomy 5q22.2
- Familial polyposis coli due to monosomy 5q22.2

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 developmental defect during embryogenesis
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.