NF1基因突变或基因内缺失所致神经纤维瘤病1型
ORPHA:363700· ICD-10 Q85.0· Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
- 遗传方式
- Autosomal dominant
- 发病年龄
- Infancy, Neonatal
ORPHA:363700· ICD-10 Q85.0· Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion