| MSS | Marshall-Smith syndrome; massage; Medical Superintendents' Society; Medicare Statistical System; men... |
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| SS | disulfide; sacrosciatic; saline soak; saline solution; saliva sample; saliva substitute; Salmonella-... |
| CDH | 1) Chronic Daily Headache = CTH = ... |
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| Dittrich's stenosis | Narrowing of the outflow tract of the right ventricle below the pulmonic valve; may be due to a localised fibrous diaphragm just below the valve or, more commonly, to a long narrow fibromuscular channel. Synonym: Dittrich's stenosis. (05 Mar 2000) |
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| double aortic stenosis | Subaortic stenosis associated with stenosis of the valve itself, both lesions being congenital. (05 Mar 2000) |
| infundibular stenosis | Narrowing of the outflow tract of the right ventricle below the pulmonic valve; may be due to a localised fibrous diaphragm just below the valve or, more commonly, to a long narrow fibromuscular channel. Synonym: Dittrich's stenosis. (05 Mar 2000) |
| oesophageal stenosis | Stricture of the oesophagus. (12 Dec 1998) |
| tricuspid stenosis | Pathologic narrowing of the orifice of the tricuspid valve. (05 Mar 2000) |
| tricuspid valve stenosis | The pathologic narrowing of the orifice of the tricuspid valve. (12 Dec 1998) |
| fish-mouth mitral stenosis | Extreme mitral stenosis. (05 Mar 2000) |
| laryngeal stenosis | Narrowing or stricture of any or all areas of the larynx; may be congenital or acquired. (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) |