OMOP Concept 4159966
Upshaw-Schulman syndrome
StandardConditionSNOMED373420004Disorder
Maps from
6
Descendants
0
Valid from
31 Jul 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Upshaw-Schulman syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143655 | Congenital thrombocytopenic purpura | Non-standard |
| ICD9CM | 287.33 | Congenital and hereditary thrombocytopenic purpura | Non-standard |
| Nebraska Lexicon | 267535004 | Congenital thrombocytopenic purpura | Non-standard |
| Nebraska Lexicon | 373420004 | Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome | Non-standard |
| Read | D313100 | Congenital thrombocytopenic purpura | Non-standard |
| Read | D313111 | Hereditary thrombocytopenia NEC | Non-standard |
Synonyms
Alternative names recorded for Upshaw-Schulman syndrome across source vocabularies.
- Congenital ADAMTS-13 deficiency
- deficiencia congénita de ADAMTS-13
- Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome
- Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome
- Familial TTP/HUS
- púrpura trombocitopénica trombótica familiar/síndrome urémico hemolítico
- síndrome de Upshaw-Schulman
- síndrome de Upshaw-Schulman (trastorno)
- TTP/HUS hereditaria
- Upshaw-Schulman syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(80)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cardiovascular system hereditary disorder
- 1Hereditary disorder of the integument
- 1Hereditary red blood cell disorder
- 1Inherited platelet disorder
- 1Thrombotic thrombocytopenic purpura
- 2Autosomal hereditary disorder
- 2Disorder of cardiovascular system
- 2Disorder of integument
- 2Hereditary disorder by system
- 2Hereditary disorder of cellular element of blood
- 2Platelet disorder
- 2Red blood cell disorder
- 2Thrombocytopenic purpura
- 2Thrombotic microangiopathy
- 3Arterial thrombosis
- 3Capillary thrombosis
- 3Cardiovascular finding
- 3Disorder of arteriole
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Disorder of hemostatic system
- 3Hereditary disease
- 3Integumentary system finding
- 3Microangiopathic hemolytic anemia
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