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Familial adenomatous polyposis due to 5q22.2 microdeletion
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
3 OMIM references -
2 associated genes
No signs/symptoms info
Familial adenomatous polyposis due to 5q22.2 microdeletion
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

APC
(UniProt - OMIM)
 MUC1
(UniProt - OMIM)
UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APC
(0.73)
MUC1


Citations in the biomedical literature:


Familial adenomatous polyposis due to 5q22.2 microdeletion
APC
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD



Familial adenomatous polyposis due to 5q22.2 microdeletion
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

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):
- Autosomal dominant nephronophthisis
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.