Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of movement
Very frequent (80-99%)HP:0100022
Cavity within brain
Very frequent (80-99%)HP:0002132
Dilated cerebral ventricle
Very frequent (80-99%)HP:0002119
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
CP
Frequent (30-79%)HP:0100021
Epilepsy
Frequent (30-79%)HP:0001250
Hemiparesis
Frequent (30-79%)HP:0001269
Mental deficiency
Frequent (30-79%)HP:0001249
Paralysis or weakness of one side of body
Frequent (30-79%)HP:0004374
Psychomotor development deficiency
Frequent (30-79%)HP:0001263
Spastic quadriplegia
Frequent (30-79%)HP:0002510
Absence of corpus callosum
HP:0001274
Cerebral cortex atrophy
HP:0002120
Schizencephaly
HP:0010636
Quick Facts
- SNOMED CT
- 38353004
- UMLS CUI
- C0302892
- Fully Specified Name
- Congenital porencephaly (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.