Congenital absence of spleen

disorder

SNOMED 93030006CUI C0600031

Overview

Congenital absence of spleen is a disorder.

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

Related Conditions

Familial isolated congenital asplenia(child)

Agenesis of spleen(child)

Diaphragmatic hernia, short bowel, asplenia syndrome(child)

Congenital anomaly of spleen(parent)

Asplenia(parent)

Quick Facts

SNOMED CT: 93030006
UMLS CUI: C0600031
Fully Specified Name: Congenital absence of spleen (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.