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点突变所致Koolen-De Vries综合征

ORPHA:363965· ICD-10 Q87.8· Koolen-De Vries syndrome due to a point mutation

患病率
<1 / 1 000 000
遗传方式
Autosomal dominant
发病年龄
Infancy, Neonatal
ICD-10 Q87.8 →