Chromosome 15q11.2 Deletion Syndrome

Chromosome 15q11.2 Deletion Syndrome(来自ICD-11)
别称:
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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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
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MALACARDS
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15
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