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2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
10 associated genes
No signs/symptoms info
Alternating hemiplegia of childhood
Postsynaptic congenital myasthenic syndromes

ATP1A2 AGRN
ATP1A3 CHRNA1
CACNA1A CHRNB1
SLC1A3 CHRND
CHRNE
DOK7
LRP4
MUSK
RAPSN
SCN4A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNA1A
(0.68)
AGRN



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Postsynaptic congenital myasthenic syndromes
AGRN CHRNA1 CHRNB1 CHRND CHRNE DOK7
LRP4 MUSK RAPSN SCN4A



Alternating hemiplegia of childhood
Postsynaptic congenital myasthenic syndromes

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

Synonym(s):
(no synonyms)

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

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

No signs/symptoms info available.