Congenital Iodine Deficiency Syndrome, Neurological Type

Preferred Label : Congenital Iodine Deficiency Syndrome, Neurological Type;

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

NCIt definition : Congenital iodine deficiency syndrome associated with mental retardation, deaf-mutism, and abnormal gait. It results from severe maternal iodine deficiency and hypothyroidism during pregnancy.;

Codes from synonyms : E00.0;

Détails

Origin ID

C197878;

UMLS CUI

C0342203;

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