Cytoscape Web
Click node...

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Combined immunodeficiency due to ZAP70 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Combined immunodeficiency due to ZAP70 deficiency

MUC1
(UniProt - OMIM)
 ZAP70
(UniProt - OMIM)
UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MUC1
(0.52)
ZAP70


Citations in the biomedical literature:


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD
Combined immunodeficiency due to ZAP70 deficiency
ZAP70



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Combined immunodeficiency due to ZAP70 deficiency

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
- Zeta-associated-protein 70 deficiency
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.