Overview
Congenital velopharyngeal incompetence 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 palate morphology
Very frequent (80-99%)HP:0000174
Abnormality of the pharynx
Very frequent (80-99%)HP:0000600
Velopharyngeal incompetence
Very frequent (80-99%)HP:0000220
Voice abnormality
Very frequent (80-99%)HP:0001608
Deafness
Frequent (30-79%)HP:0000365
Quick Facts
- SNOMED CT
- 427791009
- UMLS CUI
- C1997202
- Fully Specified Name
- Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 5
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.