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2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Alternating hemiplegia of childhood
Dejerine-Sottas syndrome

ATP1A2 EGR2
ATP1A3 MPZ
CACNA1A PMP22
SLC1A3 PRX


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATP1A2
(0.63)
PMP22



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Dejerine-Sottas syndrome
EGR2 MPZ PMP22 PRX



Alternating hemiplegia of childhood
Dejerine-Sottas syndrome

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

Synonym(s):
- Charcot-Marie-Tooth disease type 3
- HMSN 3
- Hereditary motor and sensory neuropathy type 3
- Hypertrophic neuropathy of infancy

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: -
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 -
1 MeSH reference: C538392

No signs/symptoms info available.