Congenital iodine-deficiency syndrome, myxedematous type

Preferred Label : Congenital iodine-deficiency syndrome, myxedematous type;

Inclusion CIM-10 : Endemic hypothyroid cretinism; Endemic cretinism, myxedematous type;

Rare : true;

Diag associé à un acte (%) : 90.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E001;

UMLS CUI

C2584703;

Automatic exact mappings (from CISMeF team)
- Endemic cretinism (disorder) [SNOMED CT concept]
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 [NCIt concept]
- 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]
DO Cross reference
- congenital hypothyroidism [DO Concept]
Orphanet concepts
- Congenital hypothyroidism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Iodine Deficiency Syndrome, Myxedematous Type [NCIt concept]
- 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]

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