CD Diagnosis Abbreviation

Campomelic Dysplasia

A severe birth defect that affects the formation of the bones, genital organs, and facial features. Physical features of the condition typically include bowing of the long bones of the legs and sometimes the arms, characteristic dimpling of the skin over the abnormal bones, shortened legs, underdeveloped shoulder blades, dislocated hips, abnormally rotated feet (clubfeet), and an abnormal number of ribs.

Congenital Defects

Cone Degeneration

Celiac Disease

A malabsorption syndrome that is precipitated by the ingestion of foods containing gluten, such as wheat, rye, and barley. It is characterized by inflammation of the small intestine, loss of microvilli structure, failed intestinal absorption, and malnutrition.

Canavan disease

Canavan disease, also called Canavan–van Bogaert–Bertrand disease, is an autosomal recessive degenerative disorder that causes progressive damage to nerve cells in the brain, and is one of the most common degenerative cerebral diseases of infancy. It is caused by a deficiency of the enzyme aminoacylase 2, and is one of a group of genetic diseases referred to as a leukodystrophies.

Cowden Disease

cortical dysplasia

Coeliac Disease

Crohn disease