OMOP Concept 607076
Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia
StandardConditionSNOMED1149069001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563412 | Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia | Non-standard |
Synonyms
Alternative names recorded for Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia across source vocabularies.
- JP-HHT (juvenile polyposis with hereditary haemorrhagic telangiectasia) syndrome
- JP-HHT (juvenile polyposis with hereditary hemorrhagic telangiectasia) syndrome
- Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia
- Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia (disorder)
- síndrome de poliposis juvenil con telangiectasia hemorrágica hereditaria
- síndrome de poliposis juvenil con telangiectasia hemorrágica hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Disorder of digestive system specific to fetus OR newborn
- 1Juvenile polyposis syndrome
- 1Osler hemorrhagic telangiectasia syndrome
- 2Autosomal dominant hereditary disorder
- 2Congenital arteriovenous malformation
- 2Developmental hereditary disorder
- 2Digestive system hereditary disorder
- 2Disorder of digestive system
- 2Disorder of fetus and/or newborn
- 2Disorder of gastrointestinal tract
- 2Hamartoma
- 2Hereditary dysplasia of blood vessel
- 2Mass of digestive structure
- 2Polyp
- 2Telangiectasia disorder
- 3Autosomal hereditary disorder
- 3Cardiovascular system hereditary disorder
- 3Congenital vascular malformation
- 3Developmental disorder
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of digestive tract
- 3Gastrointestinal tract finding
- 3Hereditary disease
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