UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CE CEA CEB CEC CED CEE CEF CEL CEM CEN CEP CER CES CET CEV
selected terms: 790 page 1 of 8

1. 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine
(UMLS (NCI) C0533112) =Organic Chemical; Pharmacologic Substance
51. CEFMETAZOLE
[A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. ( MSH )] (UMLS (NCI) C0007550) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
TO BE DELETED INGREDIENT PREPARATIONS;
=CEFMETAZOLE SODIUM
2. 10^9 Cells/L
[A unit of cell concentration expressed as a number of cells in billions in unit volume equal to one liter. ( NCI )] (UMLS (NCI) C0456524) =Quantitative Concept
52. Cefobid
(UMLS (NCI) C0733366) =Organic Chemical; Antibiotic ;
3. 3'-C-Ethynylcytidine
(UMLS (NCI) C0533115) =Organic Chemical; Pharmacologic Substance
53. CEFONICID
[A second-generation cephalosporin administered intravenously or intramuscularly. Its bactericidal action results from inhibition of cell wall synthesis. It is used for urinary tract infections, lower respiratory tract infections, and soft tissue and bone infections. ( MSH )] (UMLS (NCI) C0007551) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
TO BE DELETED INGREDIENT PREPARATIONS;
=Cefonicid Monosodium
4. C elegans
[roundworm important research model in animal biology, especially for the genetic and molecular basis of development and behavior. ( CSP )] (UMLS (CSP) C0162610) =Invertebrate ;
=Nematoda;
54. CEFOPERAZONE
[Semisynthetic broad-spectrum cephalosporin with a tetrazolyl moiety that is resistant to beta-lactamase. It has been proposed especially against Pseudomonas infections. ( MSH )] (UMLS (NCI) C0007552) =Organic Chemical; Antibiotic =(6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic Acid;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFOPERAZONE SODIUM
5. C element
[common nonmetallic tetrad element with atomic symbol C, atomic number 6, and atomic weight 12.011; defining element of organic compounds. ( CSP )] (UMLS (CSP) C0007009) =Element, Ion, or Isotope =Element;
=charcoal;
55. Cefotan
(UMLS (NCI) C0007553) =Organic Chemical; Antibiotic
6. c erbA
[ ] (UMLS (CSP) C0242989) =Gene or Genome ;
56. CEFOTAXIME
[A third generation semisynthetic cephalosporin antibiotic with bactericidal activity. Cefotaxime inhibits mucopeptide synthesis by binding to and inactivating penicillin binding proteins thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of bacterial cell walls. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0007554) =Organic Chemical; Antibiotic =Cephacetrile;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTIZOXIME;
CEFTRIAXONE;
CEFUROXIME;
CEFIXIME;
CEFOTAXIME SODIUM
7. c erbB
[ ] (UMLS (CSP) C0599898) =Gene or Genome ;
57. CEFOTETAN
[A semi-synthetic, broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin antibiotic derived from cephalosporium. The bactericidal activity of cefotetan disodium is caused by an inhibition of bacterial cell wall synthesis via inhibition of cross-linking of peptidoglycans. This results in a reduction of cell wall stability and causes cell lysis. Cefotetan disodium is more active against gram-negative organisms and less active against gram-positive organisms compared to first-generation cephalosporins. ( NCI )] (UMLS (NCI) C0007555) =Organic Chemical; Antibiotic =Tetrazoles;
Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
=5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl)carbonyl)amino)-7-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-, Disodium Salt,(6R-(6alpha,7alpha))-
8. C-ERBA-ALPHA-1
[A high-affinity thyroid hormone receptor expressed in many tissues, with highest levels in the central nervous system. ( NCI )] (UMLS (NCI) C0919489) ERBA-Alpha Protein;
ERBA-Related Protein 7;
THRA;
THRA Protein;
Thyroid Hormone Receptor Alpha-1 =Amino Acid, Peptide, or Protein; Receptor
58. CEFOTIAM
[One of the CEPHALOSPORINS that has a broad spectrum of activity against both gram-positive and gram-negative microorganisms. ( MSH )] (UMLS (NCI) C0007556) =Organic Chemical; Antibiotic
9. c-erbB-1
[Epidermal growth factor receptor. The protein found on the surface of some cells and to which epidermal growth factor binds, causing the cells to divide. It is found at abnormally high levels on the surface of many types of cancer cells, so these cells may divide excessively in the presence of epidermal growth factor. ( NCI )] (UMLS (NCI) C0034802) =Amino Acid, Peptide, or Protein; Enzyme; Receptor
59. CEFOTIAM HYDROCHLORIDE
(UMLS (NCI) C0771454) =Organic Chemical; Antibiotic
10. c-erbB-2
[The ERBB2 gene encodes a putative tyrosine kinase growth factor receptor EGFR2, p185 HER2/NEU antigen, similar to the EGF receptor. The ERBB2, ERBB3, and ERBB4 genes encode heregulin/neuregulin receptors, members of the EGFR-related type I receptor tyrosine kinase subfamily. The encoded proteins form homo- and heterodimers, which complicates assignment of function: ERBB2 homodimers do not bind heregulin, but ERBB2/ERBB3 heterodimers do. Herstatin is a secreted alternative ERBB2 product, of the extracellular domain, that binds to p185ERBB2, disrupts ERBB2 dimers, reduces p185 phosphorylation, and inhibits growth. Human ERBB2 gene is located at 17p12-21. Overexpression of HER-2 correlates with poor prognosis in breast carcinoma. ( NCI )] (UMLS (NCI) C0069515) =Amino Acid, Peptide, or Protein; Enzyme; Receptor
60. CEFOXITIN
[A semisynthetic cephamycin antibiotic resistant to beta-lactamase. ( MSH )] (UMLS (NCI) C0007557) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION =CEFOXITIN SODIUM
11. c-erbB-3
[HER3/erbB3. Member of the EGF receptor (erbB) family. Receptor for NDF/heregulin (Neu differentiation factor); heterodimerizes with other type I receptor tyrosine kinases. It is overexpressed frequently in several common solid tumors, including in breast cancer. ( NCI )] (UMLS (NCI) C0072460) =Amino Acid, Peptide, or Protein; Enzyme; Receptor
61. Cefpiramide
(UMLS (NCI) C0055010) =Organic Chemical; Pharmacologic Substance ;
12. c-erbB-4
[ErbB4 heterodimerizes with other type I receptor tyrosine kinases. In the peripheral nervous system, ErbB4 helps regulate glial proliferation and acts as a signaling molecule at the neuromuscular junction. In the mature CNS, ErbB4 is expressed in cerebellar granule cells and in a subset of cells that also express the neurotransmitter: aminobutyric acid. ErbB4 is critical in cardiac development. It is overexpressed frequently in several common solid tumors, including in breast cancer. ( NCI )] (UMLS (NCI) C0214098) =Amino Acid, Peptide, or Protein; Enzyme; Receptor
62. CEFPIRAMIDE SODIUM
(UMLS (NCI) C0955901) =Organic Chemical; Antibiotic
13. c-erbB-5
(UMLS (NCI) C1333354) ERBB5 Receptor Protein Tyrosine Kinase =Amino Acid, Peptide, or Protein; Enzyme; Receptor
63. Cefpodoxime
[A third generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefpodoxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefpodoxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0055011) =Organic Chemical; Antibiotic ;
=[AM103] CEPHALOSPORINS, 3RD GENERATION;
=Cefpodoxime Proxetil;
14. c-Ets-1
[A member of the ETS family of transcription factors, ETS1 Protein is a set of 42-52 kD nuclear phosphoproteins that activate transcription by interaction with purine-rich sequences in gene promoter/enhancer regions. (from OMIM 164720 and NCI) ( NCI )] (UMLS (NCI) C0107719) =Amino Acid, Peptide, or Protein; Biologically Active Substance
64. Cefpodoxime Proxetil
[A third generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefpodoxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefpodoxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0108938) =Organic Chemical; Antibiotic ;
=CEFTIZOXIME;
Cefpodoxime =CEFPODOXIME PROXETIL 100 MG;
CEFPODOXIME PROXETIL 200 MG;
CEFPODOXIME PROXETIL 100 MG/5ML;
CEFPODOXIME PROXETIL 50 MG/5ML;
15. c-Ets-2
[A member of the ETS family of transcription factors, ETS2 Protein activity is potentiated by signaling through the RAS-RAF-MEK kinase cascade and inhibited by direct interaction with the HLH ID1 protein. (from OMIM 164740 and NCI) ( NCI )] (UMLS (NCI) C0107720) =Amino Acid, Peptide, or Protein; Biologically Active Substance
65. Cefprozil
[A semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefprozil's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefprozil inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0053882) =Organic Chemical; Antibiotic ;
=[AM102] CEPHALOSPORINS, 2ND GENERATION;
Unclassified Ingredients =CEFPROZIL 250 MG;
CEFPROZIL 250 MG/5ML;
CEFPROZIL 500 MG;
CEFPROZIL 125 MG/5ML;
16. C/EBP
[A protein which binds to enhancers having a conserved CCAAT sequence. ( NCI )] (UMLS (NCI) C0108685) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
66. CEFTAZIDIME
[A beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Ceftazidime binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, ceftazidime is more active against gram-negative bacteria and less active against gram-positive bacteria. Ceftazidine also crosses the blood-brain barrier and reaches therapeutic concentrations in the central nervous system (CNS). ( NCI )] (UMLS (NCI) C0007559) =Organic Chemical; Antibiotic =Cephaloridine;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTAZIDIME 1 GM/50ML;
CEFTAZIDIME 2 GM/50ML;
CEFTAZIDIME 1 GM;
CEFTAZIDIME 500 MG;
CEFTAZIDIME 2 GM/VIL;
CEFTAZIDIME 6 GM/VIL;
CEFTAZIDIME 10 GM;
CEFTAZIDIME 1 GM/VIL;
CEFTAZIDIME 2 GM
17. C/EBP Epsilon
[C/EBP epsilon is a CCAAT enhancer-binding protein and bZIP transcription factor uniquely expressed in, and essential for differentiation of, granulocytic progenitor cells. C/EBP epsilon forms homo- or heterodimers with other family members and expression is enhanced by retinoids. Four isoforms are expressed from different promoters and an alternate start codon. (from OMIM 600749 and NCI) ( NCI )] (UMLS (NCI) C1384540) CCAAT/Enhancer Binding Protein Epsilon;
CEBPE;
=Amino Acid, Peptide, or Protein; Biologically Active Substance
67. Ceftazidime Sodium
[A beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Ceftazidime binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, ceftazidime is more active against gram-negative bacteria and less active against gram-positive bacteria. Ceftazidine also crosses the blood-brain barrier and reaches therapeutic concentrations in the central nervous system (CNS). ( NCI )] (UMLS (NCI) C0724548) =Organic Chemical; Antibiotic ;
18. CE
[A country in Southern Asia, occupying an island in the Indian Ocean, south of India. (NCI) ( NCI )] (UMLS (NCI) C0038088) =Geographic Area
68. Ceftibuten Dihydrate
(UMLS (NCI) C0873024) CEFTIBUTEN DIHYDRATE PREPARATION;
=Organic Chemical; Pharmacologic Substance ;
=CEFTIBUTEN;
=CEFTIBUTEN DIHYDRATE 400 MG;
CEFTIBUTEN DIHYDRATE 90 MG/5ML;
CEFTIBUTEN DIHYDRATE 180 MG/5ML
19. Ce element
[element of the rare earth family of metals, atomic symbol Ce, atomic number 58, and atomic weight 140.12; a malleable metal used in industrial applications. ( CSP )] (UMLS (CSP) C0007828) =Element, Ion, or Isotope ;
=Metals, Rare Earth;
69. CEFTIZOXIME
[A semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. The drug is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms. It has few side effects and is reported to be safe and effective in aged patients and in patients with hematologic disorders. ( MSH )] (UMLS (NCI) C0007560) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =Cefpodoxime Proxetil;
5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2,3-dihydro-2-imino-4-thiazolyl)(methoxyimino)acetyl)amino)-8-oxomonosodium Salt,(6R-(6alpha,7beta(Z)))-;
20. Ce-Vi-Sol
(UMLS (NCI) C0699150) =Carbohydrate; Pharmacologic Substance; Vitamin
70. Ceftobiprole
(UMLS (NCI) C1100584) =Organic Chemical; Pharmacologic Substance
21. CEA peptide-pulsed DC vaccine
[A cancer vaccine consisting of dendritic cells harvested from a patient with cancer and pulsed or transduced with a peptide fragment of carcinoembryonic antigen (CEA), a tumor-associated antigen expressed by a wide range of cancers. When the altered dendritic cells are returned to the patient, they may stimulate the host immune system to mount a cytotoxic T-lymphocyte immune response against tumor cells expressing CEA. ( NCI )] (UMLS (NCI) C0678037) =Pharmacologic Substance; Immunologic Factor
71. CEFTRIAXONE
[An antibiotic drug used to treat infection. It belongs to the family of drugs called cephalosporin antibiotics. ( NCI )] (UMLS (NCI) C0007561) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTRIAXONE SODIUM
22. CeaVac
(UMLS (NCI) C0935951) CEA-Vac;
=Amino Acid, Peptide, or Protein; Pharmacologic Substance; Immunologic Factor
72. ceftrixone
[ ] (UMLS (CSP) C0597871) =Organic Chemical; Pharmacologic Substance
23. CEB1
[Cyclin-E Binding Protein 1, encoded by the CEB1 gene, specifically interacts with cyclin E, as well as other cyclins tested, even in the absence of p21. CDK inhibitors, however, including p21 and p27, show either weak or no interaction with CEB1. The expression of CEB1 appears to be regulated by RB and p53. CEB1 may regulate or mediate the activity of CDKs because CEB1 is highly induced when both RB and p53 are inactivated, with subsequent elevation of CDK activity. (from OMIM) ( NCI )] (UMLS (NCI) C1333182) Cyclin E-Binding Protein 1;
Cyclin-E Binding Protein 1;
hect domain and RLD 5 =Amino Acid, Peptide, or Protein; Biologically Active Substance
73. Cefuroxime Axetil
[A second generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefuroxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefuroxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0055015) =Organic Chemical; Antibiotic ;
=CEFUROXIME;
=5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 3-(((aminocarbonyl)oxy)methyl)-7-((2-furanyl(methoxyimino)acetyl)amino)-8-oxo-, Monosodium Salt(6R-(6alpha,7beta(Z)))-;
CEFUROXIME AXETIL 125 MG/5ML;
CEFUROXIME AXETIL 125 MG;
CEFUROXIME AXETIL 250 MG;
CEFUROXIME AXETIL 500 MG;
CEFUROXIME AXETIL 250 MG/5ML
24. Cebidae
[American monkeys with prehensile tail, widely separated nostrils, nonopposable thumb; many forms are omnivorous and social in families. ( CSP )] (UMLS (CSP) C0007524) =Mammal =Ceboidea;
=Saimiri;
Aotus;
74. Celebes ape
[ ] (UMLS (CSP) C0205802) =Mammal ;
25. Ceboidea
[superfamily that includes all the New World monkeys, consisting of the families Callitrichidae and Cebidae. ( CSP )] (UMLS (CSP) C0596281) =Mammal ;
=Anthropoidea;
=Callithricidae;
Cebidae
75. celebrex
[ ] (UMLS (CSP) C0719198) =Organic Chemical; Pharmacologic Substance ;
26. Cebuella
[Pigmy marmosets, sometimes considered a separate genus. ( MSH )] (UMLS (CSP) C0007525) =Mammal
76. celebrity
[Celebrities are people of public interest (VIP) including employees, whose information require special protection. ( HL7V3.0 )] (UMLS (HL7) C1550475) =Idea or Concept =ConfidentialityModifiers;
27. Cecal
[A blind pouch-like commencement of the colon in the right lower quadrant of the abdomen at the end of the small intestine and the start of the large intestin ( NCI )] (UMLS (NCI) C0007531) =Body Part, Organ, or Organ Component ;
=Body Part;
77. Celecoxib + Exemestane
(UMLS (NCI) C1328011) Celecoxib/Exemestane =Therapeutic or Preventive Procedure ;
28. Cecal Lymphoma
(UMLS (NCI) C1332867) Cecum Lymphoma;
Lymphoma of Cecum;
Lymphoma of the Cecum;
Primary Cecum Lymphoma =Neoplastic Process ;
78. Celecoxib + Gefitinib
(UMLS (NCI) C1328040) Celecoxib/Gefitinib =Therapeutic or Preventive Procedure ;
29. Cecal Non-Hodgkin's Lymphoma
(UMLS (NCI) C1332868) Cecum Non-Hodgkin Lymphoma;
Cecum Non-Hodgkin's Lymphoma;
Non-Hodgkin's Lymphoma of Cecum;
Non-Hodgkin's Lymphoma of the Cecum;
Primary Cecum Non-Hodgkin's Lymphoma;
=Neoplastic Process ;
79. Celecoxib/Cisplatin/Fluorouracil
(UMLS (NCI) C1134474) =Therapeutic or Preventive Procedure
30. Cecal Villous Adenoma
(UMLS (NCI) C1332869) Cecum Villous Adenoma;
Villous Adenoma of Cecum;
Villous Adenoma of the Cecum;
=Neoplastic Process
80. Celecoxib/Cyclophosphamide/Doxorubicin/Etoposide/Ifosfamide/Vinblastine/Vincristine
(UMLS (NCI) C1327983) =Therapeutic or Preventive Procedure ;
31. CECECTOMY
[ ] (UMLS (ICD9CM) C0585458) =Therapeutic or Preventive Procedure
81. Celecoxib/Cyclophosphamide/Etoposide/Thalidomide
(UMLS (NCI) C1327787) =Therapeutic or Preventive Procedure ;
32. Cecenu
(UMLS (NCI) C1450043) =Organic Chemical; Pharmacologic Substance
82. Celecoxib/Docetaxel
(UMLS (NCI) C1134572) =Therapeutic or Preventive Procedure
33. cecostomy
[Surgical creation of an opening in the cecum. ( NCI )] (UMLS (NCI) C0007530) =Therapeutic or Preventive Procedure
83. Celecoxib/Docetaxel/Irinotecan
(UMLS (NCI) C1327925) =Therapeutic or Preventive Procedure; ;
34. CecostomyRoute
[Cecostomy ( HL7V3.0 )] (UMLS (HL7) C1699452) =Functional Concept =RouteBySite;
=Instillation, cecostomy
84. Celecoxib/Eflornithine
(UMLS (NCI) C1134612) =Therapeutic or Preventive Procedure
35. cecropin
[Antimicrobial peptides that form channels in membranes that are more permeable to anions than cations. They resemble MAGAININS, with their N-terminal region forming a positively charged amphipathic alpha helix, but containing an additional C-terminal segment. ( MSH )] (UMLS (CSP) C0597874) =Antibiotic ;
85. Celecoxib/Epirubicin
(UMLS (NCI) C1327924) =Therapeutic or Preventive Procedure ;
36. Cecum obstruction
(UMLS (NCI) C1391753) Cecum Obstruction Adverse Event =Finding ;
86. Celecoxib/Erlotinib
(UMLS (NCI) C1327971) =Therapeutic or Preventive Procedure ;
37. Ced5, C. Elegans, Homolog of
[Dedicator of Cyto-Kinesis 1, encoded by the human DOCK1 gene, binds to the SH3 domain of CRK protein and may be involved in integrin signaling. It may regulate cell surface extension. During programmed cell death (apoptosis), cell corpses are rapidly engulfed. This engulfment process involves the recognition and subsequent phagocytosis of cell corpses by engulfing cells. This protein may function in the cell surface extension of an engulfing cell around a dying cell during apoptosis. (From LocusLink, OMIM and NCI) ( NCI )] (UMLS (NCI) C1333263) Dedicator of Cyto-Kinesis 1;
DOCK, 180-kD;
DOCK1;
DOCK180;
Downstream of CRK-Binding Protein, 180-kD =Amino Acid, Peptide, or Protein; Biologically Active Substance
87. Celecoxib/Fluorouracil/Irinotecan/Leucovorin Calcium
(UMLS (NCI) C1327990) =Therapeutic or Preventive Procedure ;
38. Cedarville Rancheria, California
(UMLS (HL7) C1554255) =Population Group =NativeEntityContiguous;
88. Celecoxib/Fluorouracil/Leucovorin Calcium
(UMLS (NCI) C1328089) =Therapeutic or Preventive Procedure ;
39. CeeNU
(UMLS (NCI) C0699181) =Organic Chemical; Pharmacologic Substance ;
89. Celecoxib/Fluorouracil/Leucovorin Calcium/Oxaliplatin
(UMLS (NCI) C1328088) =Therapeutic or Preventive Procedure ;
40. CEF
(UMLS (NCI) C0060133) =Therapeutic or Preventive Procedure ;
90. Celecoxib/Gemcitabine
(UMLS (NCI) C1328033) =Therapeutic or Preventive Procedure; ;
41. CEFACLOR
[A beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity. Cefaclor binds to and inactivates penicillin-binding proteins (PBP) located in bacterial cytoplasmic membranes. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0007537) =Organic Chemical; Antibiotic =cephalexin;
[AM102] CEPHALOSPORINS, 2ND GENERATION =CEFACLOR MONOHYDRATE;
CEFACLOR 250 MG;
CEFACLOR 187 MG/5ML;
CEFACLOR 375 MG;
CEFACLOR 500 MG;
CEFACLOR 375 MG/5ML;
CEFACLOR 125 MG/5ML;
CEFACLOR 250 MG/5ML;
91. Celecoxib/Selenium
(UMLS (NCI) C0879517) =Therapeutic or Preventive Procedure ;
42. Cefadyl
(UMLS (NCI) C0733791) =Organic Chemical; Antibiotic ;
92. Celecoxib/Temozolomide/Thalidomide
(UMLS (NCI) C1327793) =Therapeutic or Preventive Procedure ;
43. Cefamandole Nafate
[The sodium salt form of cefamandole formyl ester. Cefamandole nafate is a pro-drug that is hydrolyzed by plasma esterases to produce cefamandole, a semi-synthetic beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity. Cefamandole binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0054995) =Organic Chemical; Antibiotic ;
=(6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic Acid;
=CEFAMANDOLE NAFATE 1 GM;
CEFAMANDOLE NAFATE 1 GM/VIL;
CEFAMANDOLE NAFATE 2 GM/VIL;
CEFAMANDOLE NAFATE 2 GM
93. Celecoxib/Trastuzumab
(UMLS (NCI) C0935696) =Therapeutic or Preventive Procedure
44. Cefdinir
[A semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefdinir's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefdinir inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0060405) =Organic Chemical; Antibiotic =[AM103] CEPHALOSPORINS, 3RD GENERATION;
Unclassified Ingredients =CEFDINIR 125 MG/5ML;
CEFDINIR 300 MG
94. Celecoxib/Vinorelbine
(UMLS (NCI) C1328119) =Therapeutic or Preventive Procedure; ;
45. Cefepime
[A drug used to treat infection. It belongs to the family of drugs called cephalosporin antibiotics. ( NCI )] (UMLS (NCI) C0055003) =Organic Chemical; Antibiotic ;
=[AM104] CEPHALOSPORINS, 4TH GENERATION;
Unclassified Ingredients =Cefepime Hydrochloride;
95. Celestone
(UMLS (NCI) C0701247) =Steroid; Pharmacologic Substance
46. Cefepime Hydrochloride
[The hydrochoride salt of a semi-synthetic, beta-lactamase-resistant, fourth-generation cephalosporin antibiotic derived from an Acremonium fungal species with broad-spectrum bactericidal activity. Administered parenterally, cefipime inhibits bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity, resulting in a reduction of bacterial cell wall stability and cell lysis. This agent is more active against a variety of Gram-positive pathogens compared to third-generation cephalosporins. ( NCI )] (UMLS (NCI) C0771284) CEFEPIME HYDROCHLORIDE PREPARATION;
=Organic Chemical; Antibiotic =Cefepime;
=CEFEPIME HYDROCHLORIDE 1 GM;
CEFEPIME HYDROCHLORIDE 2 GM;
CEFEPIME HYDROCHLORIDE 500 MG;
96. CELIAC ART COMPRESS SYN
(UMLS (ICD9CM) C0152098) =Disease or Syndrome ;
47. CEFIXIME
[A broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell wall synthesis by disrupting peptidoglycan synthesis, resulting in a reduction in bacterial cell wall stability and bacterial cell lysis. Stable in the presence of a variety of beta-lactamases, this agent is more active against gram-negative bacteria and less active against gram-positive bacteria compared to second-generation cephalosporins. ( NCI )] (UMLS (NCI) C0060400) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFIXIME 100 MG/5ML;
CEFIXIME 200 MG;
CEFIXIME 400 MG;
97. celiac disease
[disease occurring in children and adults characterized by sensitivity to gluten, with chronic inflammation and atrophy of the mucosa of the upper small intestine; manifestations include diarrhea, malabsorption, steatorrhea, and nutritional and vitamin deficiencies. ( CSP )] (UMLS (CSP) C0007570) =Disease or Syndrome ;
=gastrointestinal absorption disorder;
48. Cefizox
(UMLS (NCI) C0701023) =Organic Chemical; Antibiotic ;
98. Celiac Ganglion
(UMLS (NCI) C0007571) =Body Part, Organ, or Organ Component ;
49. CEFMENOXIME
[A cephalosporin antibiotic that is administered intravenously or intramuscularly. It is active against most common gram-positive and gram-negative microorganisms, is a potent inhibitor of Enterobacteriaceae, and is highly resistant to hydrolysis by beta-lactamases. The drug has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. ( MSH )] (UMLS (NCI) C0007549) =Organic Chemical; Antibiotic
99. Celiac Lymph Node
[A lymph node at the base of the celiac artery. ( NCI )] (UMLS (NCI) C0229766) =Body Part, Organ, or Organ Component
50. CEFMENOXIME HYDROCHLORIDE
(UMLS (NCI) C0282390) =Organic Chemical; Antibiotic ;
100. Celiptium
(UMLS (NCI) C0046355) =Organic Chemical; Pharmacologic Substance

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