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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
Turcot syndrome with polyposis
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Turcot syndrome with polyposis

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
Turcot syndrome with polyposis
APC



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Turcot syndrome with polyposis

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare neurologic 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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.