Congenital Iodine Deficiency Syndrome, Mixed Type

Preferred Label : Congenital Iodine Deficiency Syndrome, Mixed Type;

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

NCIt definition : Congenital iodine deficiency syndrome associated with overlapping features of both the neurological and myxedematous variants.;

Codes from synonyms : E00.2;

Details

Origin ID

C197876;

UMLS CUI

C0342202;

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

Keyword's position in hierarchy(ies) :

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