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Late-onset autosomal recessive medullary cystic kidney disease
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Miyoshi myopathy
3 OMIM references -
2 associated genes
No signs/symptoms info
Late-onset autosomal recessive medullary cystic kidney disease
Miyoshi myopathy

FAN1
(UniProt - OMIM)
 ANO5
(UniProt - OMIM)
NPHP3
(UniProt - OMIM)
 DYSF
(UniProt - OMIM)
XPNPEP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NPHP3
(0.63)
DYSF


Citations in the biomedical literature:


Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3
Miyoshi myopathy
ANO5 DYSF



Late-onset autosomal recessive medullary cystic kidney disease
Miyoshi myopathy

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: C537480
No signs/symptoms info available.