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 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
 Synonyms & Historicals
Genetic Diseases, Inborn .
Genetic Diseases .
Genetic Disorders .
Hereditary Disease .
Inborn Genetic Diseases .
Single-Gene Defects .
Defect, Single-Gene .
Defects, Single-Gene .
Disease, Genetic .
Disease, Hereditary .
Disease, Inborn Genetic .
Diseases, Genetic .
Diseases, Hereditary .
Diseases, Inborn Genetic .
Disorder, Genetic .
Disorders, Genetic .
Genetic Disease .
Genetic Disease, Inborn .
Genetic Disorder .
Inborn Genetic Disease .
Single Gene Defects .
Single-Gene Defect .
Hereditary Diseases .
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. .