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, Genetic Disease, Hereditary 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, Genetic Disease, Inborn, Disease, Genetic, Single Gene Defects, Disorders, Genetic, Diseases, Inborn Genetic

Instance information

comment

2002 ,general; prefer /genet with specific diseases ,2002; for HEREDITARY DISEASES see HEREDITARY DISEASES 1968-2001

identifier

D030342

Instance relations