Congenital hypothyroidism

Preferred Label : Congenital hypothyroidism;

LOINC status : ACTIVE;

Synonyme UMLS : cretinism; Congenital goiter; Infantile hypothyroidism; Hypothyroidism;congenital; Congenital hypothyroidism not due to iodine deficiency; Cretinism, NOS; CHT - Congenital hypothyroidism; hypothyroidism congenital; Hypothyroidism, congenital;

UMLS MTHU# : MTHU025182;

Details

Origin ID

LP56766-6;

UMLS CUI

C0010308;

Automatic exact mappings (from CISMeF team)
- Congenital goiter [HPO term]
- Congenital goitre [MedDRA LLT]
- Congenital hypothyroidism due to iodine deficiency (disorder) [SNOMED CT concept]
- Congenital hypothyroidism without goitre [ICD-10 Sub-category (who)]
- Cretinism [PASCAL descriptor]
- Cretinism [MedDRA LLT]
- Endemic cretinism (disorder) [SNOMED CT concept]
- GOITRE CONGENITAL [WHO-ART Preferred Term]
- Goiter congenital [MedDRA LLT]
- Goitre congenital [MedDRA Preferred Term]
- METABOLIC AND NUTRITIONAL DISORDERS [WHO-ART Class]
- Primary congenital hypothyroidism without thyroid developmental anomaly [ORDO Disease]
- congenital anomaly endocrine/metabolic [ICPC-2 Rubric]
- cretinism, nos [SNOMED Notion]
- hypothyroidism [MedlinePlus Topic]
Currated CISMeF NLP mapping
- Congenital Hypothyroidism [NCIt concept]
- Congenital Iodine Deficiency Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [ICD-11 Subcategory]
- Congenital hypothyroidism [ICD-9 code]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [ORDO Disease]
- 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 [DO Concept]
- congenital hypothyroidism [Disease (Nov.)]
- congenital hypothyroidism [MeSH Descriptor]
- congenital hypothyroidism [MeSH concept]
LOINC code(s)
- Congenital hypothyroidism newborn screening comment-discussion:Txt:Pt:Bld.dot:Nar: [LOINC code]
- Congenital hypothyroidism:Imp:Pt:Bld.dot:Nom: [LOINC code]
- Congenital hypothyroidism:Imp:Pt:Bld.dot:Ord: [LOINC code]
- Secondary congenital hypothyroidism:Imp:Pt:Bld.dot:Ord: [LOINC code]
See also inter- (CISMeF)
- congenital goiter [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [ICD-9 code]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [ORDO Disease]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism (disorder) [SNOMED CT concept]
- Cretinism [MedDRA LLT]
- HYPOTHYROIDISM CONGENITAL [WHO-ART Preferred Term]
- Hypothyroidism congenital [MedDRA LLT]
- congenital hypothyroidism [DO Concept]
- congenital hypothyroidism [Disease (Nov.)]
- congenital hypothyroidism [MeSH concept]
- congenital hypothyroidism [MeSH Descriptor]
- cretinism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Congenital hypothyroidism due to iodine deficiency [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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