Cytoscape Web
Click node...

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

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

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


Citations in the biomedical literature:


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



Myxofibrosarcoma
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit

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