| SD | Sandhoff disease; senile dementia; septal defect; serologically defined; serologically detectable; s... |
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| SVD | single vessel disease; singular value decomposition; small vessel disease; spontaneous vaginal deliv... |
| WD | wallerian degeneration; well developed; well differentiated; wet dressing; Whitney Damon [dextrose];... |
| TEN | Toxic Epidermal Necrolysis |
| TSS | Toxic Shock Syndrome |
| Addison's disease | <endocrinology> A rare endocrine disease that results from the underproduction of aldosterone and cortisol (hormones) by the adrenal glands. Symptoms include weakness, low blood pressure, anaemia, low blood sugar and electrolyte abnormalities. (27 Sep 1997) |
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| adult-onset still's disease | Although Still's disease was first described in children, it is known to begin in adults. See: Still's disease. (12 Dec 1998) |
| Akabane disease | A disease of cattle, sheep and goats, caused by the Akabane virus and characterised by foetal or neonatal arthrogryposis and hydranencephaly, abortions, and foetal death; the causative virus is transmitted by mosquitoes in Japan and by the midge Culicoides brevitarsis in Australia. (05 Mar 2000) |
| akamushi disease | See Typhus, scrub. (12 Dec 1998) |
| Akureyri disease | An epidemic disease characterised by stiffness of the neck and back, headache, diarrhoea, fever, and localised muscular weakness; restricted almost exclusively to adults, affecting women more than men; probably viral in origin. Synonym: Akureyri disease, benign myalgic encephalomyelitis, epidemic myalgic encephalomyelitis, Iceland disease. (05 Mar 2000) |
| Albers-Schonberg disease | The formation of abnormally dense bone, as opposed to osteoporosis. (18 Nov 1997) |
| Albert's disease | Achillobursitis involving inflammation of the bursa between the Achilles tendon and the os calcis. Synonym: Swediauer's disease. (05 Mar 2000) |
| Albright's disease | <syndrome> The abnormal development of multiple bones, hormonal disorder and brownish skin lesions. (27 Sep 1997) |
| aleutian mink disease | A slow progressive disease of mink caused by the aleutian mink disease virus. It is characterised by poor reproduction, weight loss, autoimmunity, hypergammaglobulinaemia, increased susceptibility to bacterial infections, and death from renal failure. The disease occurs in all colour types, but mink which are homozygous recessive for the aleutian gene for light coat colour are particularly susceptible. (12 Dec 1998) |
| aleutian mink disease virus | A species of parvovirus that causes a disease in mink, mainly those homozygous for the recessive aleutian gene which determines a desirable coat colour. (12 Dec 1998) |
| alexander disease | <radiology> Dysmyelinating disease, rare, sporadic, usually presents in 1st year, gradual enlargement of head (Differential diagnosis: Canavan disease), retardation, convulsion, spasticity CT findings: decreased density of white matter, frontal lobe predominance, with or without dilated lateral ventricles Diagnosis: brain biopsy (12 Dec 1998) |
| Alexander's disease | A rare, fatal central nervous system degenerative disease of infants, characterised by psychomotor retardation, seizures, and paralysis; megaloencephaly is associated with widespread leukodystrophic changes, especially in the frontal lobes. (05 Mar 2000) |
| alkali disease | A term applied to various animal poisonings of plant and mineral origin in arid regions under the belief that they were caused by the ingestion of alkaline waters; e.g., botulism of wild ducks, caused by feeding on decayed vegetation in nearly dried-up lakes. (05 Mar 2000) |
| Almeida's disease | <microbiology> A chronic fungal infection caused by Paracoccidioides brasiliensis. It is characterised by primary pulmonary lesions with dissemination to many visceral organs. Common findings include ulcerative granuloma lesions to the buccal mucosa (inner lining of the cheek) and nasal mucosa that extend to the surrounding skin. Generalised lymphangitis is also typical. More commonly seen in South America and the tropics. (15 Nov 1997) |
| Alpers disease | Familial progressive spastic paresis of extremities with progressive mental deterioration, with development of seizures, blindness and deafness, beginning during the first year of life, and with destruction and disorganization of nerve cells of the cerebral cortex. Synonym: Alpers disease, Christensen-Krabbe disease, progressive cerebral poliodystrophy. (05 Mar 2000) |