Congenital hypothyroidism

Preferred Label : Congenital hypothyroidism;

Applies to : Congenital thyroid insufficiency; Cretinism (athyrotic) (endemic);

Exclusion : Congenital (dyshormonogenic) goiter (246.1);

Additional codes : Use additional code to identify associated intellectual disabilities;

Détails

Origin ID

243;

UMLS CUI

C0010308;

Automatic exact mappings (from CISMeF team)
- congenital anomaly endocrine/metabolic [ICPC-2 Rubric]
- hypothyroidism [MedlinePlus Topic]
Currated CISMeF NLP mapping
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [ORDO Disease]
- Congenital hypothyroidism [ICD-11 Subcategory]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [LOINC component]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism (disorder) [SNOMED CT concept]
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
- HYPOTHYROIDISM CONGENITAL [WHO-ART Preferred Term]
- Hypothyroidism congenital [MedDRA LLT]
- congenital hypothyroidism [Disease (Nov.)]
- congenital hypothyroidism [DO Concept]
- congenital hypothyroidism [MeSH Descriptor]
- congenital hypothyroidism [MeSH concept]
DO Cross reference
- congenital hypothyroidism [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism [LOINC component]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [ORDO Disease]
- Congenital hypothyroidism (disorder) [SNOMED CT concept]
- Cretinism [MedDRA LLT]
- HYPOTHYROIDISM CONGENITAL [WHO-ART Preferred Term]
- Hypothyroidism congenital [MedDRA LLT]
- congenital hypothyroidism [MeSH Descriptor]
- congenital hypothyroidism [MeSH concept]
- congenital hypothyroidism [DO Concept]
- congenital hypothyroidism [Disease (Nov.)]
- cretinism, nos [SNOMED Notion]

Position du mot-clé dans l'(les) arborescence(s) :

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