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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
Acute inflammatory demyelinating polyradiculoneuropathy

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
Acute inflammatory demyelinating polyradiculoneuropathy
PMP22



Alternating hemiplegia of childhood
Acute inflammatory demyelinating polyradiculoneuropathy

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

Synonym(s):
- AIDP
- Acute idiopathic demyelinating polyneuropathy
- Acute inflammatory polyneuropathy
- GBS, acute inflammatory demyelinating polyradiculoneuropathic form
- Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- 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: 1-9 / 100 000
Average age onset: variable
Average age of death: any age
Type of inheritance: multigenic/multifactorial

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

No signs/symptoms info available.