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2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Alternating hemiplegia of childhood
Charcot-Marie-Tooth disease type 1E

ATP1A2 PMP22
ATP1A3
CACNA1A
SLC1A3


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
Charcot-Marie-Tooth disease type 1E
PMP22



Alternating hemiplegia of childhood
Charcot-Marie-Tooth disease type 1E

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

Synonym(s):
- CMT1E
- Charcot-Marie-Tooth disease - deafness

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic 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:
1 OMIM reference -
2 MeSH references: C537986 / C538078

No signs/symptoms info available.