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2 OMIM references -
4 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Alternating hemiplegia of childhood
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss

ATP1A2 ATP1A3
ATP1A3
CACNA1A
SLC1A3


COMMON
GENES
ATP1A3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATP1A2
(0.63)
ATP1A3



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss



Alternating hemiplegia of childhood
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss

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

Synonym(s):
- CAPOS syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)

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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: C536589
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.