Overview
Congenital suprabulbar paresis 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.
Abnormal vocalization
Very frequent (80-99%)HP:0002167
Abnormality of the cranial nerves
Very frequent (80-99%)HP:0001291
Deglutition disorder
Frequent (30-79%)HP:0002015
Dysphonia
Frequent (30-79%)HP:0001618
Gastroesophageal reflux disease
Frequent (30-79%)HP:0002020
Glue ear
Frequent (30-79%)HP:0040262
Increased reflexes
Frequent (30-79%)HP:0001347
Intellectual impairment
Frequent (30-79%)HP:0100543
Jaw hyperreflexia
Frequent (30-79%)HP:0033683
respiratory infections, recurrent
Frequent (30-79%)HP:0002205
Sialorrhea
Frequent (30-79%)HP:0002307
Specific learning disability
Frequent (30-79%)HP:0001328
Tongue muscle weakness
Frequent (30-79%)HP:0000183
Childhood attention deficit/hyperactivity disorder
Occasional (5-29%)HP:0007018
Decreased size of cranium
Occasional (5-29%)HP:0000252
Epilepsy
Occasional (5-29%)HP:0001250
Quadriplegia
Occasional (5-29%)HP:0002445
Sensorineural deafness
Occasional (5-29%)HP:0000407
Difficulty articulating speech
HP:0001260
Electroencephalogram abnormal
HP:0002353
Muscle weakness
HP:0001324
Poor school performance
HP:0001249
Related Conditions
Quick Facts
- SNOMED CT
- 716335003
- UMLS CUI
- C0796204
- Fully Specified Name
- Congenital suprabulbar paresis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.