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Myxedematous form of cretinism

disorder
SNOMED 64491003CUI C1578691

Overview

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

Related Conditions

Endemic congenital iodine deficiency syndrome of myxedematous type(child)
Congenital goitre(parent)
Myxedema(parent)
Congenital hypothyroidism(parent)

Quick Facts

SNOMED CT
64491003
UMLS CUI
C1578691
Fully Specified Name
Myxedematous form of cretinism (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.