OMOP Concept 4300464
Wiskott-Aldrich autosomal dominant variant syndrome
StandardConditionSNOMED403837005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Wiskott-Aldrich autosomal dominant variant syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 403837005 | Wiskott-Aldrich autosomal dominant variant syndrome | Non-standard |
Synonyms
Alternative names recorded for Wiskott-Aldrich autosomal dominant variant syndrome across source vocabularies.
- variante autosómica dominante del síndrome de Wiskott-Aldrich
- variante autosómica dominante del síndrome de Wiskott-Aldrich (trastorno)
- Wiskott-Aldrich autosomal dominant variant syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Wiskott-Aldrich syndrome
- 2Congenital immunodeficiency disease
- 2Congenital thrombocytopenia
- 2Dense body defect
- 2Hereditary cancer-predisposing syndrome
- 2Hereditary disorder of immune system
- 2Hereditary thrombocytopenic disorder
- 2Immune thrombocytopenia
- 2Immunodeficiency associated with multiple organ system abnormalities
- 3Congenital disease
- 3Disorder of immune function
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Immunodeficiency disorder
- 3Immunodeficiency with major anomalies
- 3Inherited platelet disorder
- 3Platelet storage pool defect
- 3Thrombocytopenic disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Disorder of immune structure
- 4Genetic disease
- 4Hereditary disorder of cellular element of blood
- 4Hereditary platelet function disorder
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