Overview
Bosley Salih Alorainy syndrome 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.
Sensorineural deafness
Very frequent (80-99%)HP:0000407
Aplasia of internal carotid artery
Frequent (30-79%)HP:0005290
Central hypoventilation
Frequent (30-79%)HP:0007110
Delayed gross motor development
Frequent (30-79%)HP:0002194
Epilepsy
Occasional (5-29%)HP:0001250
Duane anomaly
HP:0009921
Horizontal supranuclear gaze palsy
HP:0007817
Related Conditions
Congenital heart disease(parent)
Multiple system malformation syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Hearing loss associated with syndrome(parent)
Cardiovascular system hereditary disorder(parent)
Developmental hereditary disorder(parent)
Congenital sensorineural hearing loss(parent)
Hereditary hearing loss(parent)
Quick Facts
- SNOMED CT
- 720567008
- UMLS CUI
- C1832216
- Fully Specified Name
- Bosley Salih Alorainy syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 7
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.