Congenital Iodine Deficiency Syndrome, Myxedematous Type

Preferred Label : Congenital Iodine Deficiency Syndrome, Myxedematous Type;

NCIt related terms : Congenital iodine-deficiency syndrome, myxedematous type;

NCIt definition : Congenital iodine deficiency syndrome associated with milder mental retardation, short stature, goiter, and hypothyroidism. It results from iodine deficiency and hypothyroidism in the fetus during late pregnancy or in the neonatal period.;

Codes from synonyms : E00.1;

Détails

Origin ID

C197877;

UMLS CUI

C2584703;

CISMeF manual mappings
- Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Congenital iodine-deficiency syndrome, myxedematous type [ICD-10 Sub-category]
- Congenital iodine-deficiency syndrome, myxoedematous type [ICD-10 Sub-category (who)]
- Congenital iodine-deficiency syndrome, myxoedematous type [ICD-11 More detail]
- myxedematous form of cretinism [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital iodine-deficiency syndrome, myxedematous type [ICD-10 Sub-category]
- Congenital iodine-deficiency syndrome, myxoedematous type [ICD-11 More detail]
- Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) [SNOMED CT concept]
- Myxedematous form of cretinism (disorder) [SNOMED CT concept]
- myxedematous form of cretinism [SNOMED Notion]
concept_is_in_subset
- mCode Elixhauser Hypothyroidism Value Set [NCIt concept]
- mCode Terminology [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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