Dyrk1a-Related Intellectual Disability Syndrome Due to 21q22.13q22.2 Microdeletion

Alias:
21q22.13q22.2 Microdeletion Syndrome
Monosomy 21q22.13q22.2
Del(21)(q22.13q22.2)
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dyrk1a-Related Intellectual Disability Syndrome Due to 21q22.13q22.2 Microdeletion, is also known as 21q22.13q22.2 microdeletion syndrome. An important gene associated with Dyrk1a-Related Intellectual Disability Syndrome Due to 21q22.13q22.2 Microdeletion is DYRK1A (Dual Specificity Tyrosine Phosphorylation Regulated Kinase 1A). Affiliated tissues include breast and pituitary, and related phenotypes are intellectual disability and gait disturbance
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
<1/1000000
1
11
--

Medical Symptom

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Description
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No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
Related Gene
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References Literature

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IF
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