Diseases caused by genetic mutations that are inherited from a parent's genome.
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.
Synonyms: Single-Gene Defects, Defects, Single-Gene, Genetic Diseases, Hereditary Disease, Genetic Disease, Diseases, Genetic, Single-Gene Defect, Genetic Diseases, Inborn, Disease, Inborn Genetic, Inborn Genetic Diseases, Genetic Disorders, Defect, Single-Gene, Inborn Genetic Disease, Disorder, Genetic, Disease, Hereditary, Hereditary Diseases, Genetic Disorder, Diseases, Hereditary, Disease, Genetic, Genetic Disease, Inborn, Single Gene Defects, Disorders, Genetic, Diseases, Inborn Genetic
Instance information
general; prefer /genet with specific diseases ,2002 ,2002; for HEREDITARY DISEASES see HEREDITARY DISEASES 1968-2001
D030342