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2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Alternating hemiplegia of childhood
Extraskeletal myxoid chondrosarcoma

ATP1A2 EWSR1
ATP1A3 NR4A3
CACNA1A TAF15
SLC1A3 TCF12
TFG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNA1A
(0.63)
TAF15



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Extraskeletal myxoid chondrosarcoma
EWSR1 NR4A3 TAF15 TCF12 TFG



Alternating hemiplegia of childhood
Extraskeletal myxoid chondrosarcoma

Synonym(s):
- AHC
- Alternating hemiplegia in childhood

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
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:
2 OMIM references -
1 MeSH reference: C536589
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.