Congenital rubella syndrome

ICD-11 code : KA62.8;

Preferred Label : Congenital rubella syndrome;

ICD-11 definition : A disease caused by an infection with the rubella virus in utero. This disease presents with symptoms depending on the timing of infection of the fetus and may present with birth defects (such as hearing loss), or intrauterine growth retardation. Transmission is by vertical transmission. Confirmation is by identification of rubella virus or detection of anti-rubella virus IgM antibodies in the neonate or infant.;

ICD-11 synonym : Gregg syndrome;

Details

Origin ID

1059053724;

Currated CISMeF NLP mapping
- Congenital Rubella [NCIt concept]
- Congenital rubella [ICD-9 code]
- Congenital rubella [MedDRA LLT]
- Congenital rubella infection [MedDRA Preferred Term]
- Congenital rubella syndrome [ORDO Disease]
- Congenital rubella syndrome [ICD-10 Sub-category]
- Congenital rubella syndrome [ICD-10 Sub-category (who)]
- Congenital rubella syndrome [MedDRA Preferred Term]
- Congenital rubella syndrome (disorder) [SNOMED CT concept]
- congenital rubella syndrome [Disease (Nov.)]
- gestational rubella syndrome [SNOMED Notion]
- rubella syndrome, congenital [MeSH Descriptor]
- rubella syndrome, congenital [MeSH concept]
ICD-10 Mapping
- Congenital rubella syndrome [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients