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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Action myoclonus - renal failure syndrome
Extraskeletal myxoid chondrosarcoma

SCARB2 EWSR1
NR4A3
TAF15
TCF12
TFG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SCARB2
(0.49)
TAF15



Citations in the biomedical literature:


Action myoclonus - renal failure syndrome
SCARB2
Extraskeletal myxoid chondrosarcoma
EWSR1 NR4A3 TAF15 TCF12 TFG



Action myoclonus - renal failure syndrome
Extraskeletal myxoid chondrosarcoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic

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

No signs/symptoms info available.