1p35.2 microdeletion syndrome

disorder

SNOMED 1228844002CUI C5679992

Overview

1p35.2 microdeletion syndrome is a disorder.

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

Related Conditions

Small stature(parent)

Developmental delay(parent)

1p partial monosomy(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Quick Facts

SNOMED CT: 1228844002
UMLS CUI: C5679992
Fully Specified Name: 1p35.2 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.