ICD-11 classes
20 Developmental anomalies
Structural developmental anomalies primarily affecting one...
Structural developmental anomalies of the circulatory system
LA90 — Structural developmental anomalies of the peripheral...
LA90.0 — Capillary malformations
LA90.00 — Hereditary haemorrhagic telangiectasia
ICD-11 LA90.00 — Hereditary haemorrhagic telangiectasia
Rendu-Osler-Weber disease, also called hereditary haemorrhagic telangiectasia (HHT), is a genetic disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal haemorrhagic telangiectasias and visceral shunting.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Capillary malformations #12161
- Genetic or developmental disorders involving lips or oral mucosa #13302
- Angiodysplasia of stomach #13654
- Angiodysplasia of small intestine #13947
- Vascular disorders of the liver #14337
- Genetic or developmental disorders involving lips or oral mucosa #15229
- Genetic syndromes affecting cutaneous vasculature #15939
- Genetic syndromes affecting cutaneous vasculature #16583
- Genetic or developmental disorders involving lips or oral mucosa #16873
- Genetic or developmental disorders involving lips or oral mucosa #22812