serw-MX  [xml]  

 DeCS Categories

C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
 Synonyms & Historicals
Eye Diseases, Hereditary .
Hereditary Eye Diseases .
Disease, Hereditary Eye .
Diseases, Hereditary Eye .
Eye Disease, Hereditary .
Hereditary Eye Disease .
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder. .
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. .