Iodotyrosine deiodination defect

disorder

SNOMED 17885001CUI C0342195

Overview

Iodotyrosine deiodination defect is a disorder.

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Hypothyroidism

HP:0000821

Poor school performance

HP:0001249

Retarded growth

HP:0001510

Thyroid goiter

HP:0000853

Related Conditions

Inherited disorder of thyroid metabolism(parent)

Recessive hereditary disorder (autosomal)(parent)

Enzymopathy(parent)

Dyshormonogenic goitre(parent)

Quick Facts

SNOMED CT: 17885001
UMLS CUI: C0342195
Fully Specified Name: Iodotyrosine deiodination defect (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.