Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
Disease Name
Aicardi's syndrome
Standard Disease Name
aicardi's syndrome
MeSH Tree
No data
ICD-10
No data
Identifiers
DO ID
No data
MeSH ID
D058540
OMIM ID
304050
UMLS ID
C0175713
HPO ID
No data
Description and Extensions
Description
NCI2016_02D:A sporadic genetic syndrome characterized by agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae. It is associated with the presence of choroid plexus neoplasms in the brain.|MSH2017_2016_08_12:A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.|JABL99:A syndrome of infantile spasms, typical bowing of the head (salaam seizures), chorioretinopathy, retarded mental and motor development, agenesis of the corpus callosum, and costovertebral anomalies.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.