Chromosome 15q11.2 Deletion Syndrome

Alias:
15q11.2 Microdeletion Syndrome
15q11.2 Bp1-Bp2 Microdeletion Syndrome
Monosomy 15q11.2
Del(15)(q11.2)
Chromosome Deletion Syndrome 15q11.2
Duplication 15q11-Q13 Syndrome
Microdeletion 15q11.2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome 15q11.2 Deletion Syndrome, also known as 15q11.2 microdeletion syndrome, is related to autism spectrum disorder and attention deficit-hyperactivity disorder, and has symptoms including ataxia, seizures and clumsiness. An important gene associated with Chromosome 15q11.2 Deletion Syndrome is DEL15Q11.2 (Chromosome 15q11.2 Deletion Syndrome), and among its related pathways/superpathways are Cell Cycle, Mitotic and Loss of Nlp from mitotic centrosomes. Affiliated tissues include cortex and heart, and related phenotypes are intellectual disability and global developmental delay

Basic Information

Inheritance
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Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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15
77
6

Medical Symptom

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Gene & Mutation

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References Literature

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