OMOP Concept 313504
Osler hemorrhagic telangiectasia syndrome
StandardConditionSNOMED21877004Disorder
Maps from
15
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Osler hemorrhagic telangiectasia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 131685 | Osler haemorrhagic telangiectasia syndrome | Non-standard |
| CIM10 | I78.0 | Hereditary haemorrhagic telangiectasia | Non-standard |
| HemOnc | 613 | Hereditary hemorrhagic telangiectasia | Non-standard |
| ICD10 | I78.0 | Hereditary haemorrhagic telangiectasia | Non-standard |
| ICD10CM | I78.0 | Hereditary hemorrhagic telangiectasia | Non-standard |
| ICD10CN | I78.0 | Hereditary haemorrhagic telangiectasia | Non-standard |
| ICD10CN | I78.000 | Hereditary haemorrhagic telangiectasia | Non-standard |
| ICD10GM | I78.0 | Hereditary haemorrhagic telangiectasia | Non-standard |
| ICD9CM | 448.0 | Hereditary hemorrhagic telangiectasia | Non-standard |
| KCD7 | I78.0 | Hereditary haemorrhagic telangiectasia | Non-standard |
| MeSH | D013683 | Telangiectasia, Hereditary Hemorrhagic | Non-standard |
| Nebraska Lexicon | 21877004 | Hereditary haemorrhagic telangiectasia | Non-standard |
| OXMIS | 448 TR | RENDU- OSLER- WEBER'S DISEASE | Non-standard |
| Read | G770.00 | Hereditary haemorrhagic telangiectasia | Non-standard |
| Read | G770.11 | Rendu - Osler - Weber disease | Non-standard |
Synonyms
Alternative names recorded for Osler hemorrhagic telangiectasia syndrome across source vocabularies.
- enfermedad de Osler - Weber - Rendu
- Hereditary haemorrhagic telangiectasia
- Hereditary hemorrhagic telangiectasia
- HHT - Hereditary haemorrhagic telangiectasia
- HHT - Hereditary hemorrhagic telangiectasia
- Osler haemorrhagic telangiectasia syndrome
- Osler hemorrhagic telangiectasia syndrome (disorder)
- Osler-Rendu-Weber disease
- Osler-Rendu-Weber syndrome
- Osler-Weber-Rendu disease
- síndrome de telangiectasia hemorrágica de Osler
- síndrome de telangiectasia hemorrágica de Osler (trastorno)
- telangiectasia hemorrágica hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital arteriovenous malformation
- 1Developmental hereditary disorder
- 1Hereditary dysplasia of blood vessel
- 1Telangiectasia disorder
- 2Autosomal hereditary disorder
- 2Cardiovascular system hereditary disorder
- 2Congenital vascular malformation
- 2Developmental disorder
- 2Hereditary disease
- 2Lesion of soft tissue
- 2Vascular disorder
- 3Blood vessel finding
- 3Congenital anomaly of cardiovascular system
- 3Congenital vascular disorder
- 3Disease
- 3Disorder of cardiovascular system
- 3Disorder of soft tissue
- 3Genetic disease
- 3Hereditary disorder by system
- 4Cardiovascular finding
- 4Clinical finding
- 4Congenital cardiovascular disorder
- 4Congenital malformation
- 4Disorder of body system
Narrower concepts
(2)Included automatically when you query with descendants.
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