| CAVD | complete atrioventricular dissociation; completion, arithmetic problems, vocabulary, following direc... |
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| CBAVD | congenital bilateral absence of vas deferens |
| CBPS | congenital bilateral perisylvian syndrome |
| CCA | cephalin cholesterol antigen; chick cell agglutination; chimpanzee coryza agent; choriocarcinoma; ci... |
| CCHD | cyanotic congenital heart disease |
| juvenile cataract | A soft cataract occurring in a child or young adult. (05 Mar 2000) |
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| umbilicated cataract | Congenital cataract in which a central white membrane replaces the nucleus. Synonym: disk-shaped cataract, life-belt cataract, umbilicated cataract. (05 Mar 2000) |
| zonular cataract | A cataract in which the opacity is limited to the cortex. Synonym: zonular cataract. (05 Mar 2000) |
| fibroid cataract | A sclerotic hardening of the capsule of the lens, following exudative iridocyclitis. (05 Mar 2000) |
| floriform cataract | A congenital cataract with opacities arranged like the petals of a flower. (05 Mar 2000) |
| lamellar cataract | A cataract in which the opacity is limited to the cortex. Synonym: zonular cataract. (05 Mar 2000) |
| furnacemen's cataract | A cataract secondary to absorption of heat by the lens, or by transmission from the adjacent iris. Synonym: furnacemen's cataract, glassworker's cataract. (05 Mar 2000) |
| life-belt cataract | Congenital cataract in which a central white membrane replaces the nucleus. Synonym: disk-shaped cataract, life-belt cataract, umbilicated cataract. (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) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |