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中文16q24.3 Microdeletion Syndrome
Alias:
Monosomy 16q24.3
Del(16)(q24.3)
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16q24.3微缺失综合症，又称为16q24.3单体型，与kbg综合症和自闭症谱系障碍有关。与16q24.3微缺失综合症相关的重要基因是ANKRD11（Ankyrin Repeat Domain Containing 11）。关联组织包括皮肤，相关表型为自闭症和突出的耳朵
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