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Action myoclonus - renal failure syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant spastic paraplegia type 13
1 OMIM reference -
1 associated gene
No signs/symptoms info
Action myoclonus - renal failure syndrome
Autosomal dominant spastic paraplegia type 13

SCARB2
(UniProt - OMIM)
 HSPD1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SCARB2
(0.49)
HSPD1


Citations in the biomedical literature:


Action myoclonus - renal failure syndrome
SCARB2
Autosomal dominant spastic paraplegia type 13
HSPD1



Action myoclonus - renal failure syndrome
Autosomal dominant spastic paraplegia type 13

Synonym(s):
(no synonyms)

Synonym(s):
- SPG13
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537485
No signs/symptoms info available.