| CHRPE | congenital hypertrophy of the retinal pigment epithelium |
|---|---|
| CHS | central hypoventilation syndrome; Chediak-Higashi syndrome; cholinesterase; chondroitin sulfate; com... |
| CIA | chemiluminescent immunoassay; chymotrypsin inhibitor activity; colony-inhibiting activity; congenita... |
| CIBHA | congenital inclusion-body hemolytic anemia |
| CLAH | congenital lipoid adrenal hyperplasia |
| disease, congenital heart | A birth defect of the heart or great blood vessels (like the aorta). (12 Dec 1998) |
|---|---|
| double congenital athetosis | A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia. Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome. (05 Mar 2000) |
| toxoplasmosis, congenital | Congenital infection with toxoplasma gondii characterised by lesions of the central nervous system. (12 Dec 1998) |
| foot deformities, congenital | Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth. (12 Dec 1998) |
| limb deformities, congenital | Congenital structural deformities of the upper and lower extremities collectively or unspecified. (12 Dec 1998) |