| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
|---|---|
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
| CAH | 1) Chronic Active Hepatitis 2) Congenital Adrenal Hyperplasia |
| CEP | Congenital Erythropoetic Porphyria(= Gnther Disease; 선천성 조혈기성 Porphyria |
| cyclic strabismus | A strabismus that appears and disappears in rhythym, most frequently at 48-hour intervals. (05 Mar 2000) |
|---|---|
| X-strabismus | Strabismus in which exotropia is more marked when looking upward or downward than when looking straight ahead. (05 Mar 2000) |
| strabismus | <clinical sign> A deviation of the eye which the patient cannot overcome. The visual axes assume a position relative to each other different from that required by the physiological conditions. The various forms of strabismus are spoken of as tropias, their direction being indicated by the appropriate prefix, as cyclo tropia, esotropia, exotropia, hypertropia and hypotropia. Also called cast, heterotropia, manifest deviation and squint. Origin: Gr. Strabismos = a squinting (18 Nov 1997) |
| strabismus deorsum vergens | An obsolete term for vertical strabismus in which the visual axis of one eye deviates downward. (05 Mar 2000) |
| strabismus sursum vergens | An obsolete term for a vertical strabismus in which the visual axis of one eye deviates upward. (05 Mar 2000) |
| divergent strabismus | <clinical sign> The outward or temporal deviation of an eye. (27 Sep 1997) |
| incomitant strabismus | Strabismus due to weakness of an ocular muscle or muscles. Synonym: incomitant strabismus. (05 Mar 2000) |
| internal strabismus | An obsolete term for esotropia (05 Mar 2000) |
| external strabismus | An obsolete term for exotropia. (05 Mar 2000) |
| kinetic strabismus | Strabismus due to spasm of an extraocular muscle. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |