| AAALAC | American Association for Accreditation of Laboratory Animal Care |
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| AALAS | American Association of Laboratory Animal Science |
| ACP | accessory conduction pathway; acid phosphatase; acyl carrier protein; American College of Pathologis... |
| AHI | active hostility index; Animal Health Institute; apnea-plus-hypopnea index |
| AMC | academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit... |
| normal animal | In research, an experimental animal that has neither suffered an attack of a particular disease nor received an injection of a specific microorganism or its toxin. (05 Mar 2000) |
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| disease models, animal | Animal disease whose pathologic mechanisms are sufficiently similar to those of a different human disease for the animal disease to serve as a model. The animal disease may be either induced or naturally occurring so long as it is not the same clinical entity as the disease for which it serves as a model. E.g., scrapie is an animal model for multiple sclerosis, which has never been found or induced in an animal. (12 Dec 1998) |
| eliminative behaviour, animal | Behaviour associated with the elimination of feces and urine from the body. (12 Dec 1998) |
| toxoplasmosis, animal | Acquired infection of non-human animals by organisms of the genus toxoplasma. (12 Dec 1998) |
| transgenic animal | Genetically engineered animalor offspring of genetically engineeredanimals. The transgenic animal usually contains material from at leaseone unrelated organism, such as from a virus, plant, or other animal. (09 Oct 1997) |
| laboratory animal science | The science and technology dealing with the procurement, breeding, care, health, and selection of animals used in biomedical research and testing. (12 Dec 1998) |
| lameness, animal | A departure from the normal gait in animals. It is also called claudication. (12 Dec 1998) |
| adiposogenital dystrophy | A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms. Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism. Origin: L. Fr. G. Dys-, bad, + trophe, nourishment (05 Mar 2000) |
| Barnes' dystrophy | A rare type of muscular dystrophy, in which muscles are often hypertrophic and stronger than normal, but later become weak and atrophic. (05 Mar 2000) |
| macular dystrophy | A group of disorders involving predominately the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the retina, retinal pigment epithelium, Bruch's membrane, choroid, or a combination of these tissues. See: Stargardt's disease, Best's disease. (05 Mar 2000) |
| map-dot-fingerprint dystrophy | Fingerprint dystrophy accompanied by map-like patterns and microcystic epithelial inclusions. (05 Mar 2000) |
| reflex sympathetic dystrophy | A syndrome of pain and tenderness, usually to a hand or foot, associated with vasomotor instability, skin changes and rapid development of bony demineralisation (osteoporosis). Frequently will follow a localised trauma, stroke or peripheral nerve injury. (27 Sep 1997) |
| reflex sympathetic dystrophy syndrome | <syndrome> A condition that features a group of typical symptoms, including pain (often burning type), tenderness, and swelling of an extremity associated with varying degrees of sweating, warmth and/or coolness, flushing, discoloration, and shiny skin. (12 Dec 1998) |
| vitreo-tapetoretinal dystrophy | Autosomal recessive bilateral peripheral and central retinoschisis with pigmentary degeneration of the retina, chorioretinal atrophy, vitreous degeneration, and night blindness. Synonym: Favre's dystrophy. (05 Mar 2000) |
| Meesman dystrophy | Epithelial dystrophy characterised by progressive cysts and opacities of the corneal epithelium, with onset in infancy. Inheritance: autosomal dominant with incomplete penetrance. Synonym: Meesman dystrophy. (22 Sep 2002) |