16p12.2 microdeletion

disorder

SNOMED 768471006CUI C4708497

Overview

16p12.2 microdeletion is a disorder.

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

Related Conditions

Deletion of part of short arm of chromosome 16(parent)

Multiple system malformation syndrome(parent)

Developmental hereditary disorder(parent)

Dominant autosomal hereditary disorder, incomplete penetrance(parent)

Quick Facts

SNOMED CT: 768471006
UMLS CUI: C4708497
Fully Specified Name: 16p12.2 microdeletion syndrome (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.