9q21.3微缺失所致神经发育不全-颅面部畸形-心脏缺损-骨骼异常综合征
ORPHA:352665· ICD-10 Q93.5· Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion
- 患病率
- <1 / 1 000 000
- 遗传方式
- Not applicable, Unknown
- 发病年龄
- Infancy, Neonatal