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

APC
(UniProt - OMIM)
 APC
(UniProt - OMIM)

COMMON
GENES 		APC


Citations in the biomedical literature:


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



Familial adenomatous polyposis due to 5q22.2 microdeletion
Turcot syndrome with polyposis

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
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.