Inborn Genetic 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.

Also Known As:

Disease, Hereditary; Hereditary Disease; Genetic Diseases, Inborn; Genetic Diseases; Genetic Disorders; Single-Gene Defects; Defect, Single-Gene; Defects, Single-Gene; Disease, Genetic; 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

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342

Kouser Karim Selected Research

Kouser Karim Research Topics

Disease

Drug/Important Bio-Agent (IBA)