All individuals in MeSH

Label Id Description
Camphanes D001892 [Crystalline saturated MONOTERPENES, precursors of borneols and CAMPHENE. ]
Camphor D002164 [A bicyclic monoterpene ketone found widely in plants, especially CINNAMOMUM CAMPHORA. It is used topically as a skin antipruritic and as an anti-infective agent. ]
Camphor 5-Monooxygenase D019475 [A soluble cytochrome P-450 enzyme that catalyzes camphor monooxygenation in the presence of putidaredoxin, putidaredoxin reductase, and molecular oxygen. This enzyme, encoded by the CAMC gene also known as CYP101, has been crystallized from bacteria and the structure is well defined. Under anaerobic conditions, this enzyme reduces the polyhalogenated compounds bound at the camphor-binding site. ]
Camping D002165 [Living outdoors as a recreational activity. ]
Campomelic Dysplasia D055036 [A rarer variant of campomelic dysplasia. The characteristics match campomelic dysplasia except that long bone curvature is not present (acampomelia). , A congenital disorder of CHONDROGENESIS and OSTEOGENESIS characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the TIBIA with dimpling of the skin over the bowed areas, malformation of the pelvis and spine, 11 pairs of ribs, hypoplastic scapulae, club feet, micrognathia, CLEFT PALATE, tracheobronchomalacia, and in some patients male-to-female sex reversal (SEX REVERSAL, GONADAL). Most patients die in the neonatal period of respiratory distress. Campomelic dysplasia is associated with haploinsufficiency of the SOX9 TRANSCRIPTION FACTOR gene. ]
Camptotheca D029769 [A plant genus of the family NYSSACEAE (sometimes classified in the CORNACEAE family). It is a source of CAMPTOTHECIN. ]
Camptothecin D002166 [An alkaloid isolated from the stem wood of the Chinese tree, Camptotheca acuminata. This compound selectively inhibits the nuclear enzyme DNA TOPOISOMERASES, TYPE I. Several semisynthetic analogs of camptothecin have demonstrated antitumor activity. ]
Campylobacter D002167 [A genus of bacteria found in the reproductive organs, intestinal tract, and oral cavity of animals and man. Some species are pathogenic. ]
Campylobacter Infections D002169 [Infections with bacteria of the genus CAMPYLOBACTER. ]
Campylobacter coli D017000 [A species of gram-negative, rod-shaped bacteria isolated from the intestinal tract of swine, poultry, and man. It may be pathogenic. ]
Campylobacter fetus D002168 [A species of bacteria present in man and many kinds of animals and birds, often causing infertility and/or abortion. ]
Campylobacter hyointestinalis D044862 [A species of CAMPYLOBACTER isolated from the INTESTINES of PIGS with proliferative ENTERITIS. It is also found in CATTLE and in CRICETINAE and can cause enteritis in humans. ]
Campylobacter jejuni D016123 [A species of bacteria that resemble small tightly coiled spirals. Its organisms are known to cause abortion in sheep and fever and enteritis in man and may be associated with enteric diseases of calves, lambs, and other animals. ]
Campylobacter lari D044863 [A species of thermophilic CAMPYLOBACTER found in healthy seagulls and causing ENTERITIS in humans. ]
Campylobacter rectus D044883 [A species of CAMPYLOBACTER isolated from cases of human PERIODONTITIS. It is a microaerophile, capable of respiring with OXYGEN. ]
Campylobacter sputorum D044884 [A species of CAMPYLOBACTER comprised of three biovars based on their reaction to CATALASE and UREASE. They have been isolated from humans, CATTLE, and SHEEP. ]
Campylobacter upsaliensis D044885 [A species of CAMPYLOBACTER isolated from DOGS; CATS; and humans. ]
Campylobacteraceae D000073557 [A large and diverse group in the order CAMPYLOBACTERALES, individual species of which grow in aerobic and anaerobic conditions as free-living, commensal, or pathogenic forms. ]
Campylobacterales D000074707 [Gram negative microaerophilic bacteria of the phylum PROTEOBACTERIA, class EPSILONPROTEOBACTERIA. ]
Camurati-Engelmann Syndrome D003966 [An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder. ]