Aplasia cutis congenita secondary to malformation syndrome (Type 9)

disorder

SNOMED 403553002CUI C1274886

Overview

Aplasia cutis congenita secondary to malformation syndrome (Type 9) is a disorder.

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

Related Conditions

Delleman-Oorthuys syndrome(child)

Aplasia cutis congenita(parent)

Quick Facts

SNOMED CT: 403553002
UMLS CUI: C1274886
Fully Specified Name: Aplasia cutis congenita secondary to malformation syndrome (Type 9) (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.