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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Late-onset autosomal recessive medullary cystic kidney disease
Muscular dystrophy, Selcen type

FAN1 BAG3
NPHP3
XPNPEP3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
XPNPEP3
(0.63)
BAG3



Citations in the biomedical literature:


Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3
Muscular dystrophy, Selcen type
BAG3



Late-onset autosomal recessive medullary cystic kidney disease
Muscular dystrophy, Selcen type

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:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.