OMOP Concept 1449226
Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
StandardConditionSNOMED1351576009Disorder
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 recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency across source vocabularies.
- Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency
- Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (disorder)
- Autosomal recessive hyperimmunoglobulin M syndrome due to mutS homolog 6 deficiency
- Hyper IgM syndrome due to MSH6
- síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de MSH6
- síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de mutador S homólogo 6
- síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de mutador S homólogo 6 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hyperimmunoglobulin M syndrome
- 1Constitutional mismatch repair deficiency syndrome
- 2Autosomal recessive hereditary disorder
- 2Hereditary cancer-predisposing syndrome
- 2Hyperimmunoglobulin M syndrome
- 2Primary immune deficiency disorder
- 3Autosomal hereditary disorder
- 3Hereditary disease
- 3Immunodeficiency disorder
- 4Disorder of immune function
- 4Genetic disease
- 5Disease
- 6Clinical finding
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