Overview
Anomaly of chromosome pair 21 is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Ring chromosome 21 syndrome(child)
Complete trisomy 21 syndrome(child)
Complete monosomy 21(child)
Deletion of part of chromosome 21(child)
Duplication of chromosome 21(child)
Tetrasomy 21(child)
Paternal uniparental disomy of chromosome 21(child)
Maternal uniparental disomy of chromosome 21(child)
Anomaly of chromosome pair(parent)
Quick Facts
- SNOMED CT
- 70156005
- UMLS CUI
- C0265483
- Fully Specified Name
- Anomaly of chromosome pair 21 (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.