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Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Myxofibrosarcoma
3 associated genes
No signs/symptoms info
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Myxofibrosarcoma

WWOX
(UniProt - OMIM)
 CREB3L1
(UniProt)
CREB3L2
(UniProt - OMIM)
FUS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
WWOX
(0.63)
FUS


Citations in the biomedical literature:


Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
WWOX
Myxofibrosarcoma
CREB3L1 CREB3L2 FUS



Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Myxofibrosarcoma

Synonym(s):
- Autosomal recessive spinocerebellar ataxia-12
- SCAR12
Synonym(s):
- Fibromyxosarcoma
- Myxoid malignant fibrous histiocytoma
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.