Overview
Paternal uniparental disomy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Paternal uniparental disomy of chromosome 20(child)
Paternal uniparental disomy of chromosome 21(child)
Paternal uniparental disomy of chromosome 1(child)
Paternal uniparental disomy of chromosome 7(child)
Paternal uniparental disomy of chromosome 5(child)
Paternal uniparental disomy of chromosome 6(child)
Paternal uniparental disomy of chromosome 13(child)
Mosaic genome-wide paternal uniparental disomy(child)
Paternal uniparental disomy of chromosome X(child)
Paternal uniparental disomy of chromosome 4(child)
Paternal uniparental disomy of chromosome 15(child)
Paternal uniparental disomy of chromosome 14(child)
Paternal uniparental disomy of chromosome 11(child)
Uniparental disomy(parent)
Quick Facts
- SNOMED CT
- 726402006
- UMLS CUI
- C4518513
- Fully Specified Name
- Uniparental disomy of paternal origin (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.