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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 papillary renal cell carcinoma
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Familial papillary renal cell carcinoma

MUC1
(UniProt - OMIM)
 MET
(UniProt - OMIM)
UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MUC1
(0.49)
MET


Citations in the biomedical literature:


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD
Familial papillary renal cell carcinoma
MET



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Familial papillary renal cell carcinoma

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal 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:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538614
No signs/symptoms info available.