| SCD | scleroderma; service-connected disability; sickle-cell disease; spinocerebellar degeneration; subacu... |
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| SMCD | senile macular choroidal degeneration; systemic mast cell disease; systemic meningococcal disease |
| URD | unspecified respiratory disease; upper respiratory disease |
| VD | vapor density; vascular disease; vasodilation, vasodilator; venereal disease; venous dilatation; ven... |
| VHD | valvular heart disease; viral hematodepressive disease |
strychnine
tazettine
thoracalgia
| Virchow's disease | A condition, either congenital or acquired, in which the head is abnormally large; usually applied to an adult skull with a capacity of over 1450 ml. Synonym: leontiasis ossea, macrocephaly, macrocephalia, megacephalia, megalocephaly, megalocephalia, Virchow's disease. Origin: mega-+ G. Kephale, head (05 Mar 2000) |
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| mechanobullous disease | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
| reiter's disease | A triad of nongonococcal urethritis followed by conjunctivitis and arthritis, of unknown aetiology. (12 Dec 1998) |
| virus X disease | A term applied to a number of virus disease's of obscure aetiology, e.g., Australian X disease (Murray Valley encephalitis). (05 Mar 2000) |
| visceral disease virus | <virology> Probably the most widespread of the Herpetoviridae group. Infected cells enlarge and have a characteristic inclusion body (composed of virus particles) in the nucleus. Causes disease only in utero (leading to abortion or stillbirth or to various congenital defects), although can be opportunistic in the immunocompromised host. Patients who have been exposed to the virus will remain cytomegalovirus IgG positive. Acronym: CMV (30 Sep 1997) |
| Pauzat's disease | Osteoplastic periostitis or fatigue fractures of the metatarsal bones, caused by excessive marching. (05 Mar 2000) |
| Pavy's disease | Cyclic or recurrent physiologic albuminuria. (05 Mar 2000) |
| Paxton's disease | Corynebacterium infection of axillary and pubic hairs with development of yellow (flava), black (nigra), or red (rubra) concretions around the hair shafts; frequently asymptomatic. Synonym: lepothrix, Paxton's disease, trichomycosis chromatica, trichomycosis nodosa, trichomycosis nodularis, trichomycosis palmellina, trichonocardiosis axillaris, trichonodosis. (05 Mar 2000) |
| pearl-worker's disease | Inflammatory hypertrophy of the bones affecting grinders of mother-of-pearl. (05 Mar 2000) |
| reportable disease | <epidemiology> Diseases, usually of an infectious nature, whose occurrence is required by law to be made known to a health officer or local government authority. (05 Dec 1998) |
| Centers for Disease Control and Prevention | <organisation> The U.S. Public health agency serving as the centre for preventing, tracking controlling and investigating the epidemiology of AIDS and other diseases. (26 Mar 1998) |
| central core disease | A congenital myopathy characterised by hypotonia, delay of motor development in infancy, and nonprogressive or slowly progressive muscle weakness; on biopsy the central core of muscle fibres stains abnormally, myofibrils are abnormally compact, and there is virtual absence of mitochondria and sarcoplasmic reticulum; histochemically, the cores are devoid of oxidative enzyme, phosphorylase, and ATPase activity; autosomal dominant inheritance, often subclinical. (05 Mar 2000) |
| central core disease of muscle | <neurology> One of the conditions that produces floppy baby syndrome. It causes hypotonia (floppiness) in the newborn baby, slowly progressive muscle weakness, and muscle cramps after exercise. Muscle biopsy shows a key diagnostic finding (absent mitochondria in the centre of many type I muscle fibres). The disease is inherited as a dominant trait. The CCD gene is on chromosome 19 (and involves ryanodine receptor-1). Inheritance: autosomal dominant. (12 Dec 1998) |
| Vogt-Spielmeyer disease | Cerebral sphingolipidosis, late juvenile type. Synonym: Vogt-Spielmeyer disease. (05 Mar 2000) |
| medullary cystic disease | <disease> A rare hereditary kidney disease characterised by the gradual loss of kidney function due to the presence of cysts in the renal medulla. Symptoms include high urine output (cannot concentrate the urine), weakness, weight loss, nocturia, fatigue and headache. There is no cure and usually progresses from chronic renal failure to end stage renal disease. (27 Sep 1997) |