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Deficiency of steroid 21-hydroxylase

disorder
SNOMED 124221007CUI C0268287

Overview

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

Related Conditions

Severe steroid 21-hydroxylase deficiency(child)
Mild steroid 21-hydroxylase deficiency(child)
Moderate steroid 21-hydroxylase deficiency(child)
Specific enzyme deficiency(parent)
Disorder of adrenal cortex(parent)
Disorder of steroid metabolism(parent)

Quick Facts

SNOMED CT
124221007
UMLS CUI
C0268287
Fully Specified Name
Deficiency of steroid 21-monooxygenase (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.