OMOP Concept 4235220
Hereditary thrombocytopenic disorder
StandardConditionSNOMED438492008Disorder
Maps from
1
Descendants
24
Valid from
31 Jan 2009
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary thrombocytopenic disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 438492008 | Hereditary thrombocytopenic disorder | Non-standard |
Synonyms
Alternative names recorded for Hereditary thrombocytopenic disorder across source vocabularies.
- Hereditary thrombocytopenic disorder (disorder)
- trastorno trombocitopénico hereditario
- trastorno trombocitopénico hereditario (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Inherited platelet disorder
- 1Thrombocytopenic disorder
- 2Hereditary disorder of cellular element of blood
- 2Platelet count below reference range
- 2Platelet disorder
- 3Cytopenia
- 3Disorder of cellular component of blood
- 3Disorder of hemostatic system
- 3Hereditary disorder by system
- 3Platelet count outside reference range
- 4Blood cell count outside reference range
- 4Disease
- 4Disorder of body system
- 4Finding of blood, lymphatics and immune system
- 4Functional finding
- 4Hereditary disease
- 4Measurement finding below reference range
- 4Platelet count - finding
- 5Clinical finding
- 5Genetic disease
- 5Hemostatic system finding
- 5Measurement finding
- 5Measurement finding outside reference range
- 6Evaluation finding
- 6Hematopoietic system finding
Narrower concepts
(24)Included automatically when you query with descendants.
- 1Autosomal dominant macrothrombocytopenia
- 1Autosomal dominant thrombocytopenia with platelet secretion defect
- 1Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect
- 1Autosomal recessive combined immunodeficiency due to WIP deficiency
- 1Bernard Soulier syndrome
- 1Congenital autosomal recessive small-platelet thrombocytopenia
- 1Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type
- 1DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
- 1DK phocomelia syndrome
- 1Fanconi's anemia
- 1Hereditary macrothrombocytopenia
- 1Hereditary thrombocytopenia with early-onset myelofibrosis
- 1Hereditary thrombocytopenia with normal platelets
- 1Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
- 1Periodic fever, immunodeficiency, thrombocytopenia syndrome
- 1Radial aplasia-thrombocytopenia syndrome
- 1Severe autosomal recessive macrothrombocytopenia
- 1Thyrocerebrorenal syndrome
- 1Wiskott-Aldrich syndrome
- 1X-linked congenital dyserythropoietic anemia with thrombocytopenia
- 1X-linked thrombocytopenia with normal platelets
- 2Estren-Dameshek anemia
- 2Fanconi anemia of complementation group C
- 2Wiskott-Aldrich autosomal dominant variant syndrome
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