| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
|---|---|
| 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... |
| STS | Serologic(al) Test(s) for Syphilis; 매독혈청시험 |
| early latent syphilis | Infection with Treponema pallidum, the organism of syphilis, after the primary and secondary phases have subsided, during the first year after infection, before any manifestations of tertiary syphilis have appeared. (05 Mar 2000) |
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| early syphilis | Primary, secondary, or early latent syphilis, before any tertiary manifestations have appeared. (05 Mar 2000) |
| endemic syphilis | Syphilis caused by organisms closely related to Treponema pallidum; spread by personal, but not necessarily venereal, contact; usually acquired in childhood, most common in areas of provery and overcrowding; rare in the United States; includes yaws, pinta and bejel. Synonym: endemic syphilis. (05 Mar 2000) |
| equine syphilis | A disease of horses and donkeys caused by trypanosoma equiperdum. The disease occurs in africa, the americas, and asia. (12 Dec 1998) |
| late benign syphilis | Late syphilis, manifested by serologic evidence of infection, but without any clinical manifestations. (05 Mar 2000) |
| late latent syphilis | Usually infectious in pregnant women only, who may pass the infection on to the foetus. (05 Mar 2000) |
| latent syphilis | Infection with Treponema pallidum, after the manifestations of primary and secondary syphilis have subsided (or were never noticed), before any manifestations of tertiary syphilis have appeared. (05 Mar 2000) |
| late syphilis | Involvement of the cardiovascular or central nervous system, or the development of a gumma in any organ, due to infection with Treponema pallidum; usually several years to 2-3 decades after the initial infection. Synonym: tertiary syphilis. (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) |