| PVOD | pulmonary vascular obstructive disease; pulmonary veno-occlusive disease |
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| RHD | radiological health data; relative hepatic dullness; renal hypertensive disease; rheumatic heart dis... |
| SCD | scleroderma; service-connected disability; sickle-cell disease; spinocerebellar degeneration; subacu... |
| SMCD | senile macular choroidal degeneration; systemic mast cell disease; systemic meningococcal disease |
| URD | unspecified respiratory disease; upper respiratory disease |
Weber-Cocayne syndrome
Weinrich et Emmerson
Whipple's triad
| castleman disease | <radiology> Angiofollicular lymph node hyperplasia, benign lymphoid hyperplasia, massively enlarged lymph nodes, mediastinum most common; rarely in mesentery, age less than 30 yrs, types: hyaline vascular (90%), asymptomatic, vascular proliferation and hyalinization, plasma cell (10%), fever, anaemia, increased sed rate, increased IgG (12 Dec 1998) |
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| Castleman's disease | Solitary masses of lymphoid tissue containing concentric perivascular aggregates of lymphocytes, occurring usually in the mediastinum or hilar region of young adults; similar changes have been reported outside the mediastinum and, if associated with interfollicular sheets of plasma cells, may progress to lymphoma or plasmacytoma. Synonym: angiofollicular mediastinal lymph node hyperplasia, Castleman's disease. (05 Mar 2000) |
| gilbert's disease | A benign familial disorder, transmitted as an autosomal dominant trait. It is characterised by low-grade chronic hyperbilirubinaemia with considerable daily fluctuations of the bilirubin level. (12 Dec 1998) |
| Gilchrist's disease | <disease> A fungal infection caused by Blastomyces dermatitidis. This rare fungal infection may produce inflammatory lesion of the skin or lungs or present as a disseminated disease to the skin, lungs, bones, liver, spleen and central nervous system. Uncommon unless patient is immunocompromised (AIDS). (27 Sep 1997) |
| Gilles de la Tourette's disease | <syndrome> Both multiple motor and one or more vocal tics present with tics occurring many times a day, nearly daily, over a period of more than one year. The onset is before age 18 and the disturbance is not due to direct physiological effects of a substance or a general medical condition. The disturbance causes marked distress or significant impairment in social, occupational, or other important areas of functioning. (dsm-IV, 1994) (12 Dec 1998) |
| cat-bite disease | Rat-bite fever, presumably spread from rats to cats and thus to humans. Synonym: cat-bite fever. (05 Mar 2000) |
| reflux disease, gastroesophageal | The stomach contents regurgitate and back up (reflux) into the oesophagus the food in the stomach is partially digested by stomach acid and enzymes. Normally, the partially digested acid content in the stomach is delivered by the stomach muscle down into the small intestine for further digestion. With oesophageal reflux, stomach acid content refluxes back up into the oesophagus, occasionally reaching the breathing passages, causing inflammation and damage to the oesophagus, as well as to the lung and larynx (the voice box). 10% of patients with gerd develop barrett's oesophagus, a risk fractor in cancer of the oesophagus. (12 Dec 1998) |
| Vidal's disease | An obsolete term for lichen simplex chronicus. (05 Mar 2000) |
| cat-scratch disease | <disease> A self-limiting bacterial infection of the regional lymph nodes (lymphadenitis) caused by afipia felis, a gram-negative bacterium recently identified as bartonella henselae. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. It results in tender and enlarged lymph glands above the site of injury. A chronic benign adenopathy, especially in children and young adults, commonly associated with a recent cat scratch or bite and caused by bacteria including Bartonella henselae and Alipia felis; the lymphadenopathy usually resolves spontaneously within a period of several months, but complications involving central nervous system, liver, spleen, lung, and skin have been seen. Synonym: benign inoculation lymphoreticulosis, benign inoculation reticulosis, cat-scratch fever, regional granulomatous lymphadenitis. (05 Mar 2000) |
| refsum disease | A chronic progressive peripheral neuropathy which is probably inherited in an autosomal recessive manner. Some of the manifestations of this disorder are atypical retinitis pigmentosa, cerebellar ataxia, and increased cerebrospinal protein levels. Excessive phytanic acid storage has been found in most cases. Onset of symptoms usually occurs in early childhood. Infantile refsum disease (see peroxisomal disorders) differs in that it also includes mental retardation, dysmorphic features, peroxisomal deficiency, and very early onset. (12 Dec 1998) |
| refsum's disease | A genetic disorder of the fatty acid phytanic acid which accumulates and causes a number of progressive problems including polyneuritis (inflammation of numerous nerves), diminishing vision (due to retinitis pigmentosa), and wobbliness (ataxia) caused by damage to the cerebellar portion of the brain (cerebellar ataxia). (12 Dec 1998) |
| Vincent's disease | <disease> An acute or recurrent form of gingivitis of young to middle-aged adults characterised by red and painful gums, fetid breath and gum destruction. Other features may include fever and enlargement of the regional lymph nodes. Pathogenesis of this condition is thought to be secondary to a fusiform bacillus and spirochetal (Treponema vincentii) microorganisms. (14 Oct 1997) |
| McArdle disease | <disease> Glycogen storage disease in which the defective enzyme is muscle phosphorylase. (18 Nov 1997) |
| McArdle-Schmid-Pearson disease | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| McArdle's disease | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |