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Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Late-onset autosomal recessive medullary cystic kidney disease
3 associated genes
No signs/symptoms info
Congenital myopathy, Paradas type
Late-onset autosomal recessive medullary cystic kidney disease

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

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


Citations in the biomedical literature:


Congenital myopathy, Paradas type
DYSF
Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3



Congenital myopathy, Paradas type
Late-onset autosomal recessive medullary cystic kidney disease

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