Congenital iodine-deficiency syndrome, unspecified

Preferred Label : Congenital iodine-deficiency syndrome, unspecified;

Inclusion CIM-10 : Endemic cretinism NOS; Congenital iodine-deficiency hypothyroidism NOS;

Diag associé à un acte (%) : 87.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E009;

UMLS CUI

C3165526;

CISMeF manual mappings
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Congenital Iodine Deficiency Hypothyroidism [NCIt concept]
Orphanet concepts
- Congenital hypothyroidism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Iodine Deficiency Hypothyroidism [NCIt concept]
- Congenital Iodine Deficiency Syndrome [NCIt concept]
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
Validated automatic mappings to BTNT
- Congenital hypothyroidism due to iodine deficiency [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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