Hereditary haemorrhagic telangiectasia

ICD-11 code : LA90.00;

Preferred Label : Hereditary haemorrhagic telangiectasia;

ICD-11 definition : Rendu-Osler-Weber disease, also called hereditary hemorrhagic telangiectasia (HHT), is a genetic disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.;

ICD-11 synonym : Osler-Weber-Rendu disease; Rendu-Osler-Weber disease; Osler haemorrhagic telangiectasia syndrome; HHT - [hereditary haemorrhagic telangiectasia];

ICD-11 acronym : HHT;

Details

Origin ID

714406192;

Automatic exact mappings (from CISMeF team)
- ACVRL1 wt Allele [NCIt concept]
- activin A receptor like type 1 [ORDO Gene]
Currated CISMeF NLP mapping
- Hereditary Hemorrhagic Telangiectasia [NCIt concept]
- Hereditary haemorrhagic telangiectasia [MedDRA Preferred Term]
- Hereditary haemorrhagic telangiectasia [ICD-10 Sub-category (who)]
- Hereditary hemorrhagic telangiectasia [MedDRA LLT]
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
- Hereditary hemorrhagic telangiectasia [ICD-10 Sub-category]
- Hereditary hemorrhagic telangiectasia [ICD-9 code]
- Osler hemorrhagic telangiectasia syndrome (disorder) [SNOMED CT concept]
- Osler-Rendu disease [PASCAL descriptor]
- Osler-Weber-Rendu disease [MedDRA LLT]
- Rendu Osler Weber syndrome [Disease (Nov.)]
- Rendu-Osler-Weber disease [TUV Concept]
- Rendu-Osler-Weber syndrome [MedDRA LLT]
- Telangiectasia, hereditary hemorrhagic, type 1 [OMIM Phenotype]
- hereditary hemorrhagic telangiectasia [DO Concept]
- osler hemorrhagic telangiectasia syndrome [SNOMED Notion]
- telangiectasia, hereditary hemorrhagic [MeSH Descriptor]
- telangiectasia, hereditary hemorrhagic [MeSH concept]
False automatic mappings
- Homoharringtonine [MeSH Descriptor]
- homoharringtonine [MeSH concept]
ICD-10 Mapping
- Hereditary hemorrhagic telangiectasia [ICD-10 Sub-category]
Validated automatic mappings to NTBT
- cardiovascular disease other [ICPC-2 Rubric]

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