| FAP | familial adenomatous polyposis; familial amyloid polyneuropathy; fatty acid polyunsaturated; fatty a... |
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| EAEC | Entero-Adherent Escherichia Coli |
| EHEC | Entero-Hemorrhagic Escherichia Coli |
| EIEC | Entero-Invasive Escherichia Coli |
| EPEC | Entero-Pathogenic Escherichia Coli |
| escherichia coli o157 | A verocytotoxin-producing serogroup belonging to the o subfamily of escherichia coli which has been shown to cause severe food-borne disease. Recently, a strain from this serogroup, serotype h7 which produces shiga-like toxins, has been linked to human disease outbreaks resulting from contamination of foods from bovine origin. This serogroup causes haemorrhagic and haemolytic uraemic syndrome and predominantly haemorrhagic diarrhoea and gastroenteritis in children. (12 Dec 1998) |
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| Escherichia coli periplasmic proteinase | <enzyme> Included in group of microbial serine proteinases, EC 3.4.21.14 Registry number: EC 3.4.21.- Synonym: E coli protease I, proteinase i (26 Jun 1999) |
| Escherichia coli RNase I | <enzyme> An enzyme endonucleolytically cleaving RNA to 3'-nucleotides with 2',3'-cyclic nucleotides as intermediates. Synonym: Escherichia coli RNase I, microbial RNase II, plant RNase, RNase N2. (05 Mar 2000) |
| tunica mucosa coli | mucosa of colon |
| tunica muscularis coli | Muscular layer of the wall of the colon. Synonym: tunica muscularis coli. (05 Mar 2000) |
| tunica serosa coli | Serous coat of the colon; the visceral peritoneum of the large intestine. Synonym: tunica serosa coli. (05 Mar 2000) |
| flexura coli dextra | The bend of the colon at the juncture of its ascending and transverse portions. Synonym: flexura coli dextra, hepatic flexure. (05 Mar 2000) |
| flexura coli sinistra | The bend at the junction of the transverse and descending colon. Synonym: flexura coli sinistra, splenic flexure. (05 Mar 2000) |
| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
| benign juvenile melanoma | A benign, slightly pigmented or red superficial small skin tumour composed of spindle-shaped, epithelioid, and multinucleated cells that may appear atypical; most common in children, but also appearing in adults. Synonym: benign juvenile melanoma, epithelioid cell nevus, spindle cell nevus. (05 Mar 2000) |
| rheumatoid arthritis, systemic-onset juvenile | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| periodontitis, juvenile | Localised periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in african americans than in other races or ethnic groups. (12 Dec 1998) |
| xanthogranuloma, juvenile | Benign disorder of infants and children characterised by multiple nodules with lipid-laden, non-langerhans-cell histiocytes. (12 Dec 1998) |
| systemic-onset juvenile chronic arthritis | See: Systemic-onset juvenile rheumatoid arthritis (still's disease). (12 Dec 1998) |
| systemic-onset juvenile rheumatoid arthritis | <rheumatology> A form of joint disease, arthritis, that presents with systemic upset. Clinical signs: high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis itself may not be immediately apparent but once apparent, it may persist after the systemic symptoms have resolved. Synonym: Still's disease. (03 Jul 1999) |