Noonan syndrome
收藏NIAID Data Ecosystem2026-05-10 收录
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资源简介：
Noonan syndrome is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations.Mutations in the PTPN11 gene cause about half of all cases. SOS1 gene mutations cause an additional 10 to 15 percent, and RAF1 and RIT1 genes each account for about 5 percent of cases.
创建时间：
2025-11-26
