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

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

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


Citations in the biomedical literature:


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



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

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