| phagocyte bactericidal dysfunction | Disorders in which phagocytic cells cannot kill ingested bacteria; characterised by frequent recurring infection with formulation of granulomas. (12 Dec 1998) |
|---|---|
| phagocyte dysfunction | Disorder in which the ability of the phagocyte to engulf and ingest particles may be impaired. (05 Mar 2000) |
| phagocytic dysfunction disorders immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| phagocytic dysfunction immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| minimal brain dysfunction | An inability to control behaviour due to difficulty in processing neural stimuli. (12 Dec 1998) |
| placental dysfunction | 1. Denoting faulty development or ripening; often connoting structural and/or functional abnormalities. 2. In obstetrics, denoting an infant whose birth weight is inappropriately low for its gestational age. 3. Immature development of the placenta so that normal function does not occur. Synonym: placental dysfunction. (05 Mar 2000) |
| placental dysfunction syndrome | <syndrome> Foetal malnutrition and hypoxia resulting from impaired transfer of oxygen and various nutritive materials from mother to foetus. (05 Mar 2000) |
| constitutional hepatic dysfunction | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| constitutional liver dysfunction | An inherited disorder that affects the way bilirubin in handled by the liver. Thought to be due to an inborn error of bilirubin metabolism. Symptoms include mild jaundice, weakness, fatigue, nausea and abdominal pain. (27 Sep 1997) |
| myofacial pain-dysfunction syndrome | <syndrome> Dysfunction of the masticatory apparatus related to spasm of the muscles of mastication precipitated by occlusal dysharmony or alteration in vertical dimension of the jaws, and exacerbated by emotional stress; characterised by pain in the preauricular region, muscle tenderness, popping noise in the temporomandibular joint, and limitation of jaw motion. Synonym: temporomandibular joint pain-dysfunction syndrome. (05 Mar 2000) |
| hereditary peroneal nerve dysfunction | <neurology> A slowly progressive genetic disorder characterised by muscle atrophy in the feet and the legs, progressing to the hands and arms, due to a disorder involving the destruction of nerves (degeneration of the myelin sheath). Other features include foot drop and a slapping gait. There is no specific treatment for this disorder. (27 Sep 1997) |
| psychosexual dysfunction | Sexual dysfunction, a disturbance of sexual functioning, e.g., impotence, premature ejaculation, anorgasmia, presumed to be of psychological rather than physical aetiology. (05 Mar 2000) |
| sphincter of Oddi dysfunction | Structural or functional abnormality of the sphincter of Oddi that interferes with bile drainage. Synonym: biliary dyskinesia. (05 Mar 2000) |
| dental dysfunction | <dentistry> Abnormal functioning of dental structures. (05 Mar 2000) |
| dysfunction | Disturbance, impairment or abnormality of the functioning of an organ. (18 Nov 1997) |