Congenital iodine-deficiency syndrome, neurological type

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

Inclusion CIM-10 : Endemic cretinism, neurological type;

Diag associé à un acte (%) : 100.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E000;

UMLS CUI

C0342203;

Currated CISMeF NLP mapping
- Congenital Iodine Deficiency Syndrome, Neurological Type [NCIt concept]
- Congenital iodine deficiency syndrome of neurological type (disorder) [SNOMED CT concept]
- Congenital iodine-deficiency syndrome, neurological type [ICD-11 More detail]
- Congenital iodine-deficiency syndrome, neurological type [ICD-10 Sub-category (who)]
Orphanet concepts
- Congenital hypothyroidism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Iodine Deficiency Syndrome, Neurological Type [NCIt concept]
- Congenital iodine deficiency syndrome of neurological type (disorder) [SNOMED CT concept]
- Congenital iodine-deficiency syndrome, neurological type [ICD-11 More detail]

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