Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form

disorder

SNOMED 840509001CUI C5395374

Overview

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

Related Conditions

Congenital anomaly of adrenal gland(parent)

Adrenocortical hyperplasia(parent)

Quick Facts

SNOMED CT: 840509001
UMLS CUI: C5395374
Fully Specified Name: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (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.