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Genetic Diseases, Inborn

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.
推出的年份: 2002
副标题
树号: C16.320
MeSH 单一 ID: D030342
进入的组:
  • Disease, Inborn Genetic
  • Diseases, Inborn Genetic
  • Genetic Disease, Inborn
  • Inborn Genetic Disease
  • Inborn Genetic Diseases
  • Hereditary Diseases
  • Hereditary Disease
  • Disease, Hereditary
  • Diseases, Hereditary
  • Genetic Disorders
  • Disorder, Genetic
  • Disorders, Genetic
  • Genetic Disorder
  • Genetic Diseases
  • Disease, Genetic
  • Diseases, Genetic
  • Genetic Disease
  • Single-Gene Defects
  • Defect, Single-Gene
  • Defects, Single-Gene
  • Single Gene Defects
  • Single-Gene Defect

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