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Transient congenital hypothyroidism due to dual oxidase 2 mutation

disorder
SNOMED 1142106007CUI C5545676

Overview

Transient congenital hypothyroidism due to dual oxidase 2 mutation is a disorder.

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

Related Conditions

Congenital hypothyroidism(parent)
Transient hypothyroidism(parent)

Quick Facts

SNOMED CT
1142106007
UMLS CUI
C5545676
Fully Specified Name
Transient congenital hypothyroidism due to dual oxidase 2 mutation (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.

Transient congenital hypothyroidism due to dual oxidase 2 mutation — Symptoms, Testing & Specialists | Ltrl