Overview
Anomaly of chromosome pair 20 is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Ring chromosome 20 syndrome(child)
Complete trisomy 20 syndrome(child)
Congenital hereditary endothelial dystrophy(child)
Maternal uniparental disomy of chromosome 20(child)
Paternal uniparental disomy of chromosome 20(child)
Deletion of part of chromosome 20(child)
Duplication of chromosome 20(child)
Mosaic trisomy chromosome 20(child)
Anomaly of chromosome pair(parent)
Quick Facts
- SNOMED CT
- 9839007
- UMLS CUI
- C0265478
- Fully Specified Name
- Anomaly of chromosome pair 20 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.