congenital hypothyroidism

Preferred Label : congenital hypothyroidism;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0005308;

UMLS CUI

C0010308;

Automatic exact mappings (from CISMeF team)
- Congenital goiter [HPO term]
- Congenital hypothyroidism without goitre [ICD-10 Sub-category (who)]
- Cretinism [MedDRA LLT]
- Endemic cretinism (disorder) [SNOMED CT concept]
- congenital anomaly endocrine/metabolic [ICPC-2 Rubric]
- cretinism, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [ICD-11 Subcategory]
- Congenital hypothyroidism [LOINC component]
- Congenital hypothyroidism [ICD-9 code]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [MedDRA Preferred 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.)]
MeSH narrower concept(s)
- endemic cretinism [MeSH concept]
- myxedema, congenital [MeSH concept]
Related record
- congenital hypothyroidism [MeSH Descriptor]
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 [LOINC component]
- 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.)]
- cretinism, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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