ICD-11 classes
20 Developmental anomalies
Structural developmental anomalies primarily affecting one...
Structural developmental anomalies of the eye, eyelid or...
LA11 — Structural developmental anomalies of the anterior segment...
9C61.4 — Developmental glaucoma
9C61.42 — Secondary childhood glaucoma
1F02 — Rubella
KA62.8 — Congenital rubella syndrome
ICD-11 KA62.8 — Congenital rubella syndrome
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.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Rubella #981
- Viral infection in the fetus or newborn #1383
- Rubella #9885
- Rubella #10483
- Prenatally acquired infections with neonatal skin manifestations #16980
- Viral infection in the fetus or newborn #21751
- Syndromes with multiple structural anomalies, without predominant body system involvement #23428
- Conditions with disorders of intellectual development as a relevant clinical feature #23735