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

FAN1
(UniProt - OMIM)
 ATXN1
(UniProt - OMIM)
NPHP3
(UniProt - OMIM)
XPNPEP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NPHP3
(0.63)
ATXN1


Citations in the biomedical literature:


Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3
Spinocerebellar ataxia type 1
ATXN1



Late-onset autosomal recessive medullary cystic kidney disease
Spinocerebellar ataxia type 1

Synonym(s):
(no synonyms)

Synonym(s):
- SCA1
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: 1-9 / 100 000
Average age onset: variable
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.