Congenital iodine deficiency syndrome of mixed type

disorder

SNOMED 237565000CUI C0342202

Overview

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

Related Conditions

Congenital iodine deficiency syndrome of neurological type(parent)

Endemic congenital iodine deficiency syndrome of myxedematous type(parent)

Quick Facts

SNOMED CT: 237565000
UMLS CUI: C0342202
Fully Specified Name: Congenital iodine deficiency syndrome of mixed 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.