Paternal uniparental disomy of chromosome 21

disorder

SNOMED 766720000CUI C4707801

Overview

Paternal uniparental disomy of chromosome 21 is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Paternal uniparental disomy(parent)

Anomaly of chromosome pair 21(parent)

Quick Facts

SNOMED CT: 766720000
UMLS CUI: C4707801
Fully Specified Name: Paternal uniparental disomy of chromosome 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.

Paternal uniparental disomy of chromosome 21 — Symptoms, Testing & Specialists | Ltrl | Healos