Congenital Iodine Deficiency Hypothyroidism

Preferred Label : Congenital Iodine Deficiency Hypothyroidism;

NCIt definition : Thyroid hormone deficiency present at birth and caused by iodine deficiency.;

Details

Origin ID

C27116;

UMLS CUI

C3165526;

Automatic exact mappings (from CISMeF team)
- Endemic cretinism (disorder) [SNOMED CT concept]
- cretinism, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital hypothyroidism [LOINC component]
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
- Congenital iodine-deficiency syndrome [ICD-10 category (who)]
- Congenital iodine-deficiency syndrome [ICD-10 category]
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category (who)]
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Thyroid Gland [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
- Congenital iodine-deficiency syndrome [ICD-10 category]
- Congenital iodine-deficiency syndrome [ICD-10 category (who)]
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category]
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category (who)]
disease_has_normal_tissue_origin
- Thyroid Gland Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Thyroid Gland [NCIt concept]

Keyword's position in hierarchy(ies) :

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