Congenital hypothyroidism

ICD-11 code : 5A00.0;

Preferred Label : Congenital hypothyroidism;

ICD-11 definition : Hypothyroidism is a condition where the thyroid gland produces too little or no thyroid hormone, and the condition arises at birth. Common clinical features include decreased activity and increased sleep, feeding difficulty and constipation, prolonged jaundice, myxedematous facies, large fontanels (especially posterior), macroglossia, a distended abdomen with umbilical hernia, and hypotonia.;

ICD-11 "other" category code : 5A00.0Y;

ICD-11 "unspecified" category code : 5A00.0Z;

Details

Origin ID

602450215;

Automatic exact mappings (from CISMeF team)
- congenital anomaly endocrine/metabolic [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism [ICD-9 code]
- Congenital hypothyroidism [LOINC component]
- 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 [MeSH Descriptor]
- congenital hypothyroidism [DO Concept]
- congenital hypothyroidism [MeSH concept]
ICD-10 Mapping
- Hypothyroidism, unspecified [ICD-10 Sub-category]
Validated automatic mappings to BTNT
- Endemic cretinism (disorder) [SNOMED CT concept]
- cretinism, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- Hypothyroidism, unspecified [ICD-10 Sub-category]

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