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2 OMIM references -
4 associated genes
No signs/symptoms info
COMMON GENES: 2
PROTEIN INTERACTIONS: 2
4 OMIM references -
4 associated genes
9 signs/symptoms
Alternating hemiplegia of childhood
Familial or sporadic hemiplegic migraine

ATP1A2 ATP1A2
ATP1A3 CACNA1A
CACNA1A PRRT2
SLC1A3 SCN1A


COMMON
GENES
ATP1A2
CACNA1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATP1A2
ATP1A3
(0.63)
(0.63)
CACNA1A
ATP1A2



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Familial or sporadic hemiplegic migraine
PRRT2 SCN1A



Alternating hemiplegia of childhood
Familial or sporadic hemiplegic migraine

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

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: 1-5 / 10 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

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

Familial or sporadic hemiplegic migraine

Very frequent
- Autosomal dominant inheritance
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Movement disorder

Frequent
- Ataxia / incoordination / trouble of the equilibrium
- Nystagmus

Occasional
- EEG anomalies
- Retinitis pigmentosa / retinal pigmentary changes
- Sensorineural deafness / hearing loss
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia


Alternating hemiplegia of childhood

(no data available)