Hereditary hemorrhagic telangiectasia

Preferred Label : Hereditary hemorrhagic telangiectasia;

Inclusion CIM-10 : Rendu-Osler-Weber disease;

Diag associé à un acte (%) : 80.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

I780;

UMLS CUI

C0039445;

Currated CISMeF NLP mapping
- Hereditary Hemorrhagic Telangiectasia [NCIt concept]
- Hereditary haemorrhagic telangiectasia [MedDRA Preferred Term]
- Hereditary haemorrhagic telangiectasia [ICD-10 Sub-category (who)]
- Hereditary haemorrhagic telangiectasia [ICD-11 Sub-sub category]
- Hereditary hemorrhagic telangiectasia [MedDRA LLT]
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
- 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 (see also primary pulmonary hypertension ({ps178600}) [OMIM phenotypic series]
- Telangiectasia, hereditary hemorrhagic, type 1 [OMIM Phenotype]
- hereditary hemorrhagic telangiectasia [DO Concept]
- osler hemorrhagic telangiectasia syndrome [SNOMED Notion]
- telangiectasia, hereditary hemorrhagic [MeSH concept]
- telangiectasia, hereditary hemorrhagic [MeSH Descriptor]
DO Cross reference
- hereditary hemorrhagic telangiectasia [DO Concept]
False automatic mappings
- Homoharringtonine [MeSH Descriptor]
- homoharringtonine [MeSH concept]
Orphanet concepts
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Hemorrhagic Telangiectasia [NCIt concept]
- Hereditary haemorrhagic telangiectasia [MedDRA Preferred Term]
- Hereditary hemorrhagic telangiectasia [MedDRA LLT]
- Hereditary hemorrhagic telangiectasia [ICD-9 code]
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
- 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]

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