| CFFA | cystic fibrosis factor activity |
|---|---|
| CFS | cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; cr... |
| CFTR | cystic fibrosis transmembrane conductance regulator |
| CHF | chick embryo fibroblast; chronic heart failure; congenital hepatic fibrosis; congestive heart failur... |
| CIPF | classic interstitial pneumonitis-fibrosis; clinical illness promoting factor |
| idiopathic myelofibrosis | A progressive disease of the bone marrow where neoplastic bone marrow stem cells lodge and grow in multiple sites outside the bone marrow. Typically, there is enlargement of the spleen and a gradual replacement of the bone marrow elements by fibrosis (scarring), progressive anaemia and variable changes in the number of white blood cells and platelets. Diagnosis is by bone marrow biopsy. There is no definitive treatment for this disorder that has been shown to affect life span favorably. (27 Sep 1997) |
|---|---|
| idiopathic neuralgia | <symptom> Nerve pain not due to any apparent cause. (05 Mar 2000) |
| idiopathic orthostatic hypotension | <clinical sign> The tendency for blood pressure to drop for unknown reasons on assuming upright posture. (05 Mar 2000) |
| idiopathic paroxysmal rhabdomyolysis | Excretion of myoglobin in the urine; results from muscle degeneration, which releases myoglobin into the blood; occurs in certain types of trauma (crush syndrome), advanced or protracted ischemia of muscle, or as a paroxysmal process of unknown aetiology. Synonym: idiopathic paroxysmal rhabdomyolysis, Meyer-Betz disease, Meyer-Betz syndrome. (05 Mar 2000) |
| idiopathic proctitis | Probably a variant of ulcerative colitis involving the rectum; some cases progress to involve the remainder of the colon as well. Synonym: chronic ulcerative proctitis. (05 Mar 2000) |
| idiopathic pulmonary haemosiderosis | <chest medicine> A rare, sporadic, fatal, mostly in children with an equal sex distribution. The condition also occurs in adults where there is a sex difference (M:F = 2:1). The patients present with recurrent attacks of pulmonary haemorrhage, acute phase: bat-wing alveolar infiltrates, clears rapidly, chronic findings: haemosiderosis, pulmonary fibrosis, cor pulmonale. (12 Dec 1998) |
| idiopathic pulmonary hypertension | <chest medicine> A condition where there is increased blood pressure in the pulmonary arteries with otherwise normal heart and lungs. The cause is unknown, but there is diffuse narrowing of the pulmonary arteries resulting in increased arteriolar pressures. Secondary heart failure ensues without correction of this problem. There is an increased incidence of this disease in females between the ages of 20 and 40 years. Treatment may include a heart and lung transplant in select cases. (27 Sep 1997) |
| idiopathic roseola | Roseola not occurring as a symptom of a recognised general disease. (05 Mar 2000) |
| idiopathic thrombocytopenia purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| idiopathic thrombocytopenic purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| dystonia, idiopathic torsion | A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. (12 Dec 1998) |
| oesophageal spasm, diffuse | A motor disorder of the oesophagus characterised by chest pain and dysphagia. Pathogenesis is unclear. Strong, nonpropulsive contractions of the oesophagus evoked by deglutition occur, especially in the elderly. (12 Dec 1998) |
| t-lymphocytopenia, idiopathic CD4-positive | Reproducible depletion of CD4+ lymphocytes below 300 per cubic millimeter in the absence of HIV infection or other known causes of immunodeficiency. This is a rare, heterogeneous syndrome and does not appear to be caused by a transmissible agent. (12 Dec 1998) |
| jaundice, chronic idiopathic | A familial chronic form of nonhemolytic jaundice thought to be due to a defect in the excretion of conjugated bilirubin and certain other organic anions (e.g., sulfobromophthalein) by the liver. It is characterised by the presence of a brown, coarsely granular pigment in the hepatic cells, which is pathognomonic of the condition. (12 Dec 1998) |
| keratoderma, palmoplantar, diffuse | An autosomal dominant disorder characterised by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (keratoderma, palmoplantar), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present. (12 Dec 1998) |