| combined version | Bipolar version by means of one hand in the vagina, the other on the abdominal wall. (05 Mar 2000) |
|---|---|
| congenital severe combined immunodeficiency | Disease, one form of which is caused by the lack of a transcription factor required for expression of HLA class II genes. (18 Nov 1997) |
| contraceptives, oral, combined | Fixed drug combinations administered orally for contraceptive purposes. (12 Dec 1998) |
| severe combined immunodeficiency | Group of rare congenital disorders characterised by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an x-linked or autosomal recessive defect. About half of the patients with autosomal recessive scid are deficient in the enzyme adenosine deaminase. (12 Dec 1998) |
| severe combined immunodeficient mice | Mice that lack both T and B lymphocytes and are used for transplantation and study of human lymphoid tissues resulting in a SCID-human mouse chimera. See: severe combined immunodeficiency. (05 Mar 2000) |
| hyperlipidemia, familial combined | A disorder genetically distinct from the other inherited hyperlipidemias characterised by the type II or type IV lipoprotein pattern (the pattern may change from time to time and the lipid level may be normal at one time and abnormal at another time). (12 Dec 1998) |
| subacute combined degeneration of the spinal cord | A subacute or chronic disorder of the spinal cord, such as that occurring in certain patients with vitamin B12 deficiency, characterised by a slight to moderate degree of gliosis in association with spongiform degeneration of the posterior and lateral columns. Synonym: combined sclerosis, combined system disease, funicular myelitis, Putnam-Dana syndrome, vitamin B12 neuropathy. (05 Mar 2000) |
| the combined tendinous expansions of the sartorius | Gracilis, and semitendinosus muscles at the medial border of the tuberosity of the tibia. (05 Mar 2000) |
| familial combined hyperlipemia | familial hyperlipoproteinemia |
| familial combined hyperlipidaemia | <biochemistry, endocrinology> Inherited as a defective gene, this disorder is characterised by elevations in serum cholesterol and/or triglycerides. There are often multiple types of lipoproteins (LDL) elevated in one family. This condition is associated with an increased risk of cardiovascular disease. (27 Sep 1997) |
| basilar impression | An invagination of the base of the skull into the posterior fossa with compression of the brainstem and cerebellar structures into the foramen magnum. Compare: platybasia. (05 Mar 2000) |
| cardiac impression of liver | A depression on the superior area of the diaphragmatic surface of the liver corresponding to the position of the heart. Synonym: impressio cardiaca hepatis. (05 Mar 2000) |
| cardiac impression of lung | The depression on the medial surface of each lung produced by the presence of the heart. It is more pronounced on the left lung. Synonym: impressio cardiaca pulmonis. (05 Mar 2000) |
| gastric impression | A hollow on the visceral surface of the left lobe of the liver corresponding to the location of the stomach. Synonym: impressio gastrica. (05 Mar 2000) |
| partial denture impression | An impression or negative copy of all or a part of the partially edentulous dental arch or area, made for the purpose of designing or constructing a partial denture. (05 Mar 2000) |