| type V acrocephalosyndactyly | Acrocephalosyndactyly with broad short thumbs and great toes, often with duplication (polydactyly) of the great toes and variable syndactyly of other digits; autosomal dominant inheritance. Synonym: Pfeiffer's syndrome. (05 Mar 2000) |
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| type V familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of chylomicrons, VLDL, pre-beta-lipoproteins, and triglycerides, and slight rise of cholesterol on a normal diet, with beta-lipoproteins normal; may be accompanied by bouts of abdominal pain, hepatosplenomegaly, susceptibility to atherosclerosis, and abnormal glucose tolerance; probably autosomal recessive inheritance. Synonym: combined fat-and carbohydrate-induced hyperlipaemia, familial hyperchylomicronaemia with hyperprebetalipoproteinaemia, mixed hyperlipaemia. (05 Mar 2000) |
| type VIII mucopolysaccharidosis | <syndrome> An autosomal recessive disorder due to a deficiency of a beta-glucuronidase; defective lysosomal degradation of dermatan sulfate, heparan sulfate, and chondroitin sulfate; cellular function disrupted in most tissues. Synonym: type VII mucopolysaccharidosis, type VIII mucopolysaccharidosis. (05 Mar 2000) |
| type VII mucopolysaccharidosis | <syndrome> An autosomal recessive disorder due to a deficiency of a beta-glucuronidase; defective lysosomal degradation of dermatan sulfate, heparan sulfate, and chondroitin sulfate; cellular function disrupted in most tissues. Synonym: type VII mucopolysaccharidosis, type VIII mucopolysaccharidosis. (05 Mar 2000) |
| type VI mucopolysaccharidosis | <biochemistry, syndrome> An error of mucopolysaccharide metabolism due to deficiency of the lysosomal enzyme arylsulphatase B. It is characterised by excretion of dermatan sulfate in the urine, growth retardation, lumbar kyphosis, sternal protrusion, genu valgum, usually hepatosplenomegaly, and no mental retardation. Onset occurs after two years of age. Inheritance: autosomal recessive. Synonym: polydystrophic dwarfism, mucopolysaccharidosis type VI. (05 Mar 2000) |
| type V mucopolysaccharidosis | Former designation for Scheie's syndrome. (05 Mar 2000) |
| Farr type assay | <investigation> Method of radioimmunoassay in which free antigen remains soluble and antibody antigen complexes are precipitated. (18 Nov 1997) |
| undifferentiated type fever | A term applied to illnesses resulting from infection by any one of the arboviruses pathogenic for man, in which the only constant manifestation is fever; rash, lymphadenopathy, or arthralgia (alone or in combination) may occur in some individuals but not in others; some arboviruses may induce infections in which undifferentiated type fever is the only manifestation, whereas other arboviruses may induce in some persons only undifferentiated fever, and in other persons similar fever followed by secondary manifestations, e.g., a haemorrhagic fever or encephalitis. (05 Mar 2000) |
| "e"-type cholinesterase | <enzyme, neurology, physiology> An enzyme that breaks down unused acetylcholine in the synaptic cleft (the space between neurons), this enzyme is necessary to restore the synaptic cleft so it is ready to transmit the next nerve impulse. (06 May 1997) |
| Langhans'-type giant cells | Multinucleated giant cell's seen in tuberculosis and other granulomas; the nuclei are arranged in an arciform manner at the periphery of the cell's. Synonym: Langhans'-type giant cells. Synonym: cytotrophoblastic cells. (05 Mar 2000) |
| Laron type dwarfism | Dwarfism associated with an absent or very low levels of somatomedin C (insulin-like growth factor I) or abnormalities in receptor activity. (05 Mar 2000) |
| F-type ATPase | <enzyme> One of three major classes of ion transport ATPase, characterised by a multi subunit structure and a lack of a phosphorylated intermediate. See: ATP synthase, P-type ATPase, V-type ATPase. (18 Nov 1997) |
| accessory cephalic vein | <anatomy, vein> A variable vein that passes along the radial border of the forearm to join the cephalic vein near the elbow. Synonym: vena cephalica accessoria. (05 Mar 2000) |
| accessory hemiazygos vein | <anatomy, vein> Formed by the union of the fourth to seventh left posterior intercostal veins, passes along the side of the bodies of the fifth, sixth, and seventh thoracic vertebrae, then crosses the midline behind the aorta, oesophagus, and thoracic duct, and empties into the azygos vein, sometimes in common with the hemiazygos vein. Synonym: vena hemiazygos accessoria, vena azygos minor superior. (05 Mar 2000) |
| accessory saphenous vein | <anatomy, vein> An occasional vein running in the thigh parallel to the great saphenous vein which it joins just before the latter empties into the femoral vein. Synonym: vena saphena accessoria. (05 Mar 2000) |