OMOP Concept 1449222
Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency
StandardConditionSNOMED1351570003Disorder
Maps from
0
Descendants
0
Valid from
1 Nov 2024
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency across source vocabularies.
- Autosomal dominant activation-induced cytidine deaminase deficiency
- Autosomal dominant hyper IgM syndrome due to AICDA
- Autosomal dominant hyper-IgM syndrome type 2
- Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
- Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)
- síndrome de hiper-IgM autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación
- síndrome de hiperinmunoglobulina M autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación
- síndrome de hiperinmunoglobulina M autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection
- 2Autosomal hereditary disorder
- 2Combined immunodeficiency disease
- 2Hyperimmunoglobulin M syndrome
- 3Hereditary disease
- 3Primary immune deficiency disorder
- 4Genetic disease
- 4Immunodeficiency disorder
- 5Disease
- 5Disorder of immune function
- 6Clinical finding
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