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Familial adenomatous polyposis due to 5q22.2 microdeletion
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Multiple paragangliomas associated with polycythemia
1 associated gene
No signs/symptoms info
Familial adenomatous polyposis due to 5q22.2 microdeletion
Multiple paragangliomas associated with polycythemia

APC
(UniProt - OMIM)
 EPAS1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APC
(0.63)
EPAS1


Citations in the biomedical literature:


Familial adenomatous polyposis due to 5q22.2 microdeletion
APC
Multiple paragangliomas associated with polycythemia
EPAS1



Familial adenomatous polyposis due to 5q22.2 microdeletion
Multiple paragangliomas associated with polycythemia

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):
- Multiple paragangliomas associated with erythrocytosis
- Paraganglioma - somatostatinoma - polycythemia
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
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: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.