osler hemorrhagic telangiectasia syndrome - CISMeF

CISMeF

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Osler hemorrhagic telangiectasia syndromeSNOMED Notion

Preferred Label : osler hemorrhagic telangiectasia syndrome;

Details

Origin ID

D4-01041;

UMLS CUI

C0039445;

Automatic exact mappings (from CISMeF team)
- cardiovascular disease other [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Hereditary Hemorrhagic Telangiectasia [NCIt concept]
- Hereditary haemorrhagic telangiectasia [ICD-11 Sub-sub category]
- Hereditary haemorrhagic telangiectasia [ICD-10 Sub-category (who)]
- Hereditary haemorrhagic telangiectasia [MedDRA Preferred Term]
- Hereditary hemorrhagic telangiectasia [ICD-10 Sub-category]
- Hereditary hemorrhagic telangiectasia [ICD-9 code]
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
- Hereditary hemorrhagic telangiectasia [MedDRA LLT]
- 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]
- telangiectasia, hereditary hemorrhagic [MeSH Descriptor]
- telangiectasia, hereditary hemorrhagic [MeSH concept]
False automatic mappings
- Homoharringtonine [MeSH Descriptor]
- homoharringtonine [MeSH concept]
ICD-10 exact mapping(s)
- Hereditary haemorrhagic telangiectasia [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Conjunctival telangiectasia [ORDO Disease]
- Genetic skin vascular disorder [ORDO Disease]
- Genetic vascular anomaly [ORDO Disease]
- Malformation syndrome with hamartosis [ORDO Disease]
- Neurovascular malformation [ORDO Disease]
- Rare capillary malformation [ORDO Disease]
- Rare developmental defect with skin/mucosae involvement [ORDO Disease]
- Rare systemic disease [ORDO Disease]
- Skin vascular disease [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Osler hemorrhagic telangiectasia syndrome (disorder) [SNOMED CT concept]
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 haemorrhagic telangiectasia [ICD-10 Sub-category (who)]
- Hereditary hemorrhagic telangiectasia [ICD-9 code]
- Hereditary hemorrhagic telangiectasia [ICD-10 Sub-category]
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
- Hereditary hemorrhagic telangiectasia [MedDRA LLT]
- 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]
- telangiectasia, hereditary hemorrhagic [MeSH Descriptor]
- telangiectasia, hereditary hemorrhagic [MeSH concept]

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15/06/2025

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