Steroid 21-monooxygenase deficiency, simple virilizing type

disorder

SNOMED 52604008CUI C0268287

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Virilizing syndrome of adrenal origin(parent)

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency(parent)

Quick Facts

SNOMED CT: 52604008
UMLS CUI: C0268287
Fully Specified Name: Steroid 21-monooxygenase deficiency, simple virilizing type (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.