Schizencephaly

disorder

SNOMED 253159001CUI C0266484

Overview

Schizencephaly is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Cavity within brain

Very frequent (80-99%)HP:0002132

Electroencephalogram abnormal

Very frequent (80-99%)HP:0002353

Hypoplastic or absent corpus callosum

Very frequent (80-99%)HP:0007370

Involuntary muscle stiffness, contraction, or spasm

Very frequent (80-99%)HP:0001257

Squint

Very frequent (80-99%)HP:0000486

Cognitive delay

Frequent (30-79%)HP:0001263

Epilepsy

Frequent (30-79%)HP:0001250

Hemiparesis

Frequent (30-79%)HP:0001269

Mental deficiency

Frequent (30-79%)HP:0001249

Spastic quadriplegia

Frequent (30-79%)HP:0002510

Absence of corpus callosum

HP:0001274

Cerebral cortex atrophy

HP:0002120

Schizencephaly

HP:0010636

Related Conditions

Congenital anomaly of cerebrum(parent)

Lesion of brain(parent)

Disorder of neuronal migration and differentiation(parent)

Quick Facts

SNOMED CT: 253159001
UMLS CUI: C0266484
Fully Specified Name: Schizencephaly (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.