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Intermittent hydrarthrosis
2 associated genes
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
Intermittent hydrarthrosis
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

MEFV
(UniProt - OMIM)
 MUC1
(UniProt - OMIM)
TNFRSF1A
(UniProt - OMIM)
 UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TNFRSF1A
(0.63)
MUC1


Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD



Intermittent hydrarthrosis
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal dominant nephronophthisis
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
(no data available)
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.