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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
4 associated genes
No signs/symptoms info
CLN11 disease
Alternating hemiplegia of childhood

GRN ATP1A2
ATP1A3
CACNA1A
SLC1A3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


CLN11 disease
GRN
Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3



CLN11 disease
Alternating hemiplegia of childhood

Synonym(s):
(no synonyms)

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

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.