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Infantile epileptic-dyskinetic encephalopathy
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Early infantile epileptic encephalopathy
Micrencephaly - corpus callosum agenesis - abnormal genitalia
Partington syndrome
Spasticity - intellectual deficit - X-linked epilepsy
West syndrome
X-linked lissencephaly with abnormal genitalia
X-linked non-syndromic intellectual deficit
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ARX Q96QS3300382
No signs/symptoms info available.