这个词是什么意思？
Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D030342 · MeSH 2026。
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