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
T T T, T- T0 T1 T2 T3 T4 T9 TA TB TC TD TE TF TG TH TI TJ TK TL TM TN TO TP TQ TR TS TT TU TV TW TY TZ
TH TH2 THA THB THC THE THI THL THO THP THR THU THY
selected terms: 452 page 1 of 5

1. (-)-Thalidomide
[piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn due to teratogenic effects; it has been reintroduced and used for a number of immunological and inflammatory disorders. ( CSP )] (UMLS (NCI) C0039736) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance =[CN100] ANALGESICS;
[CN300] SEDATIVES/HYPNOTICS;
phthalimide;
Piperidones;
Teratogen;
[IM900] IMMUNOLOGICAL AGENTS, OTHER =THALIDOMIDE 50 MG;
THALIDOMIDE 100 MG;
THALIDOMIDE 200 MG
51. The indicated appointment is booked
(UMLS (HL7) C1548409) =Intellectual Product =Filler status codes;
2. *Threshold Mass Concentration
(UMLS (HL7) C1264644) =Quantitative Concept =Kind of quantity;
52. The indicated appointment was deleted from the filler application
(UMLS (HL7) C1548413) =Intellectual Product =Filler status codes;
3. *Threshold Substance Concentration
(UMLS (HL7) C1264646) =Quantitative Concept =Kind of quantity;
53. The indicated appointment was discontinued (DC'ed while in progress, discontinued parent appointment, or discontinued child appointment)
(UMLS (HL7) C1548412) =Intellectual Product =Filler status codes;
4. 1,1'-Thiobis(2-chloroethane)
[A pale yellow, oily, highly toxic, volatile, liquid alkylating compound with a sweet to garlic-like odor that evaporates to a poisonous gas. Mustard gas is a vesicant that was first used in chemical warfare in World War I, but is now only used in small amounts in research studies involving alkylating agents. Exposure to this substance is corrosive to the eyes, skin and lungs and leads to blindness and blistering of the skin and can cause severe and sometimes fatal respiratory damage. Mustard gas is a mutagen and is a known carcinogen that is associated with an increased risk of developing lung and other respiratory tract cancers. (NCI05) ( NCI )] (UMLS (NCI) C0026874) =Organic Chemical; Hazardous or Poisonous Substance ;
54. The indicated appointment was stopped from occurring (canceled prior to starting)
(UMLS (HL7) C1548410) =Intellectual Product =Filler status codes;
5. 1,3, 4-Thiadiazol-2-amine (9CI)
[A synthetic derivative of nicotinamide adenine dinucleotide (NAD). Aminothiadiazole competitively inhibits inosine 5-monophosphate dehydrogenase, thereby disrupting the regulation of cell proliferation and differentiation in a number of cells. This agent is also a selective human adenosine A3 receptor antagonist. (NCI04) ( NCI )] (UMLS (NCI) C0092419) =Organic Chemical; Pharmacologic Substance
55. The indicated time slot(s) is(are) blocked
(UMLS (HL7) C1548408) =Intellectual Product =Filler status codes;
6. 2,4 thiazolidinedione
[ ] (UMLS (CSP) C0289779) =Organic Chemical; Pharmacologic Substance ;
56. The last service request in a cyclic group.
(UMLS (HL7) C1548963) =Idea or Concept =Cyclic Entry/Exit Indicator;
7. 2-Thiophenecarboxylic Acid, 4-Methyl-3-((1-oxo-2-(propylamino)propyl)amino)-, Methyl Ester, Monohydrochloride
[The hydrochloride salt form of articaine, an amide-type local anesthetic. Articaine hydrochloride reversibly blocks nerve impulse conduction by binding to specific membrane sodium ion channels thereby interfering with the electrical excitation in the nerve, slowing the propagation of the nerve impulse and reducing the rate of rise of the action potential. This results in a loss of sensation at the injection site. Articaine hydrochloride is used for relief of pain in minor operations, usually in combination with the vasoconstrictor epinephrine. ( NCI )] (UMLS (NCI) C0007300) =Organic Chemical; Pharmacologic Substance ;
57. the number pi
[3,14159 ( HL7V3.0 )] (UMLS (HL7) C1551049) =Quantitative Concept =UnitOfMeasureAtomInsens;
UnitOfMeasureAtomSens
8. 2-Thiourea
[(NH2)2C=S; precursor and metabolite of 2-thiouracil, used for similar purposes. ( CSP )] (UMLS (NCI) C0039958) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid =sulfur compound;
58. The patient did not show up for the appointment
(UMLS (HL7) C1548414) =Intellectual Product =Filler status codes;
9. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 3,3-dimethyl-7-oxo-, 4,4-dioxide, Sodium Salt,(2S-cis)-
[The sodium salt form of sulbactam, a beta-lactam with weak antibacterial property. Sulbactam sodium contains a beta-lactam ring and irreversibly binds to beta-lactamase at or near its active site, thereby blocking enzyme activity and preventing metabolism of other beta-lactam antibiotics. Combining this agent with a beta-lactamase sensitive antibiotic such as penicillins and cephalosporins against penicillinase-producing and beta-lactamase-producing organisms, results in a decreased turnover rate of the sensitive antibiotic and enhances its antibacterial property. ( NCI )] (UMLS (NCI) C0282355) =Organic Chemical; Antibiotic ;
=SULBACTAM;
=SULBACTAM SODIUM 1.5 GM/VIL;
SULBACTAM SODIUM 3 GM/VIL;
SULBACTAM SODIUM 5 GM;
59. The primary diagnosis
(UMLS (HL7) C0332137) =Qualitative Concept =Diagnosis Priority;
10. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-,(2S-(2alpha,5alpha,6beta))-, Monosodium Salt
[The sodium salt form of benzylpenicillin, a semi-synthetic, broad-spectrum penicillin antibiotic with bactericidal activity. Benzylpenicillin sodium 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) C0037540) =Organic Chemical; Antibiotic ;
=Penicillin G Benzathine;
PENICILLIN G PROCAINE;
PENICILLIN;
=PENICILLIN G SODIUM 5000000 UNT
60. the primary procedure
(UMLS (HL7) C1547223) =Idea or Concept =Procedure Priority;
11. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-, Monopotassium Salt
[The potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic. Penicillin G potassium binds to penicillin binding proteins (PBP), the enzymes that catalyze the synthesis of peptidoglycan, which is a critical component of the bacterial cell wall. This leads to the interruption of cell wall synthesis, consequently leading to bacterial cell growth inhibition and cell lysis. ( NCI )] (UMLS (NCI) C0700462) =Organic Chemical; Antibiotic =Penicillin G Benzathine;
PENICILLIN G PROCAINE;
PENICILLIN;
=PENICILLIN G POTASSIUM 40000 UNT/ML;
PENICILLIN G POTASSIUM 20000 UNT/ML;
PENICILLIN G POTASSIUM 30000 UNT/ML;
PENICILLIN G POTASSIUM 5000000 UNT;
PENICILLIN G POTASSIUM 20000000 UNT;
PENICILLIN G POTASSIUM 1000000 UNT;
61. The printable 7-bit ASCII character set.
(UMLS (HL7) C1546818) =Intellectual Product =Alternate character sets;
12. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-(((1-aminocyclohexyl)carbonyl)amino)-3,3-dimethyl-7-oxo-,(2S-(2alpha,5alpha,6beta))-
[A semi-synthetic beta-lactam aminocyclohexylpenicillin antibiotic. Cyclacillin is bactericidal and binds to specific penicllin-binding proteins, thereby inhibiting transpeptidation during peptidoglycan synthesis. This leads to an interruption of the bacterial cell wall, causing instability of bacterial cell wall and results in cell lysis. Cyclacillin is beta-lactamase susceptible. ( NCI )] (UMLS (NCI) C0010523) =Organic Chemical; Antibiotic ;
=Penicillanic Acid;
[AM052] PENICILLINS, AMINO DERIVATIVES
62. The printable characters from the ISO 8859/1 Character set
(UMLS (HL7) C1546809) =Intellectual Product =Alternate character sets;
13. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-((2,6-dimethoxybenzoyl)amino)-3,3-dimethyl-7-oxo-, Monosodium Salt, Monohydrate,(2S-(2alpha,5alpha,6beta))-
[The sodium salt form of methicillin, a semisynthetic beta-lactam penicillin antibiotic with beta-lactamase resistant activity. Methicillin sodium is bactericidal and binds to specific penicillin-binding proteins on the bacterium and inhibits the transpeptidation enzyme, thereby preventing the cross-linking of peptidoglycans. This leads to an interruption of the bacterial cell wall and causes bacterial lysis. Methicillin sodium is active against beta-lactamase producing staphylococci. ( NCI )] (UMLS (NCI) C0887175) Celbenin;
METHICILLIN SODIUM;
METHICILLIN SODIUM PREPARATION;
=Organic Chemical; Antibiotic ;
=2,6 dimethoxyphenylpenicillin;
63. The printable characters from the ISO 8859/2 Character set
(UMLS (HL7) C1546810) =Intellectual Product =Alternate character sets;
14. 4-Thiazolidine Carboxylic Acid
[A cyclic sulfur amino acid derivative with potential antineoplastic and antioxidant activity. Thiazolidine carboxylic acid (TCA) acts on cellular membranes of malignant cells through an unknown mechanism to induce reverse transformation, a term denoting changes in morphological and growth characteristics that cause malignant cells to revert back to an untransformed state. TCA produces anti-proliferative effects by restoring contact inhibition, a phenomenon characterized by the paracrine inhibition of mitosis following the formation of a critical cell mass, which is presumably the result of cell-to-cell signal transfer. This drug may also produce antioxidant effects secondary to its release of cysteine and restoration of glutathione concentrations, an important protective property useful against DNA-damaging agents, including chemotherapy and radiation. ( NCI )] (UMLS (NCI) C0076425) =Organic Chemical; Pharmacologic Substance
64. The printable characters from the ISO 8859/3 Character set
(UMLS (HL7) C1546811) =Intellectual Product =Alternate character sets;
15. 4-Thiazolidinecarboxamide, N-(1,1-dimethylethyl)-3- [2-hydroxy-3-[[2-[[(5-isoquinolinyloxy)acetyl]amino]-3- (methylthio)-1-oxopropyl]amino]-1-oxo-4-phenylbutyl]-,[4R-[3[2S*, 3S*(R*)],4R*]]
[A synthetic peptide-based antiviral agent. As a peptidomimetic substrate containing an unnatural amino acid, allophenylnorstatine, KNI-272 selectively binds to and inhibits the human immunodeficiency virus (HIV) 1 and 2 proteases, thereby preventing cleavage of the gag-pol viral polyprotein and resulting in the release of immature, noninfectious virions. (NCI04) ( NCI )] (UMLS (NCI) C0174543) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
65. The printable characters from the ISO 8859/4 Character set
(UMLS (HL7) C1546812) =Intellectual Product =Alternate character sets;
16. 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)))-
[The sodium salt form of cefuroxime and a semi-synthetic, broad-spectrum, beta-lactamase resistant, second-generation cephalosporin antibiotic with bactericidal activity. Cefuroxime sodium inhibits bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. Lack of cross-linking results in a reduction of cell wall stability and leads to cell lysis. ( NCI )] (UMLS (NCI) C0701852) =Organic Chemical; Antibiotic =CEFUROXIME;
Cefuroxime Axetil =Cefuroxime 1.5 MG/ML Injectable Solution;
CEFUROXIME SODIUM 7.5 GM/VIL;
CEFUROXIME SODIUM 30 MG/ML;
CEFUROXIME SODIUM 15 MG/ML;
CEFUROXIME SODIUM 7.5 MG/ML;
CEFUROXIME SODIUM 7.5 GM;
CEFUROXIME SODIUM 750 MG
66. The printable characters from the ISO 8859/5 Character set
(UMLS (HL7) C1546813) =Intellectual Product =Alternate character sets;
17. 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)))-
[The sodium salt form of ceftizoxime and a semi-synthetic, broad-spectrum, beta-lactamase resistant, third-generation cephalosporin antibiotic with bactericidal activity. Ceftizoxime sodium inhibits bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. Lack of cross-linking results in a reduction of cell wall stability and leads to cell lysis. ( NCI )] (UMLS (NCI) C0282391) =Organic Chemical; Antibiotic ;
=CEFTIZOXIME;
=ceftizoxime 1 gm injectable powder for injection;
ceftizoxime 10 gm injectable powder for injection;
CEFTIZOXIME SODIUM 2 GM/VIL;
CEFTIZOXIME SODIUM 20 MG/ML;
CEFTIZOXIME SODIUM 40 MG/ML;
CEFTIZOXIME SODIUM 1 GM;
CEFTIZOXIME SODIUM 2 GM;
CEFTIZOXIME SODIUM 500 MG
67. The printable characters from the ISO 8859/6 Character set
(UMLS (HL7) C1546814) =Intellectual Product =Alternate character sets;
18. 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-3-((1Z)-2-(4-methyl-5-thiazolyl)ethenyl)-8-oxo-,2,2-dimethyl-1-oxopropoxy)methyl Ester,(6R,7R)-
[A semi-synthetic, broad-spectrum, beta-lactamase resistant, third-generation cephalosporin antibiotic with bactericidal activity. Cefditoren pivoxil is a prodrug that is rapidly hydrolyzed by intestinal esterases during absorption to the microbiologically active cefditoren, an active aminothiazolyl cephalosporin. Cefditoren inactivates penicillin binding proteins (PBPs) thereby interfering with peptidoglycan synthesis and inhibiting bacterial cell wall synthesis. Another consequence of beta-lactam exposure results in the loss of lipoteichoic acids from the cell wall. Lipoteichoic acids inhibit murein hydrolase activity and their absence from the cell wall triggers uncontrolled autolytic activity rendering bacterial cells susceptible to osmotic shock. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0245519) =Organic Chemical; Antibiotic ;
=CEFDITOREN;
Unclassified Ingredients
68. The printable characters from the ISO 8859/7 Character set
(UMLS (HL7) C1546815) =Intellectual Product =Alternate character sets;
19. 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))-
[The disodium salt form of cefotetan and a semi-synthetic, broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin antibiotic with bactericidal activity. Cefotetan disodium causes inhibition of bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0700471) =Organic Chemical; Antibiotic =CEFOTETAN;
=CEFOTETAN DISODIUM 1 GM/VIL;
CEFOTETAN DISODIUM 2 GM/VIL;
CEFOTETAN DISODIUM 1 GM/50ML;
CEFOTETAN DISODIUM 2 GM/50ML;
CEFOTETAN DISODIUM 10 GM/VIL;
CEFOTETAN DISODIUM 2 GM;
CEFOTETAN DISODIUM 1 GM;
69. The printable characters from the ISO 8859/8 Character set
(UMLS (HL7) C1546816) =Intellectual Product =Alternate character sets;
20. 6 thiopurine riboside
[ ] (UMLS (CSP) C0599534) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance
70. The printable characters from the ISO 8859/9 Character set
(UMLS (HL7) C1546817) =Intellectual Product =Alternate character sets;
21. TH
[A country in Southeastern Asia, bordering the Andaman Sea and the Gulf of Thailand, southeast of Burma. (NCI) ( NCI )] (UMLS (NCI) C0039725) =Geographic Area
71. The Read Codes Four Byte Set:
[The Read Codes Four Byte Set consists of 4 alphanumeric characters. This version contains approximately 40,000 codes arranged in a hierarchical structure. Top level hierarchy sections: DisordersFindings Surgical proceduresInvestigationsOccupationsDrugs ( HL7V3.0 )] (UMLS (HL7) C1553863) =Intellectual Product =CodeSystem;
22. Th1 cell
[Type 1 Helper Cells are a subset of helper-inducer T-lymphocytes which synthesize and secrete interleukin-2, gamma-interferon, and interleukin-12. Due to their ability to kill antigen-presenting cells and their lymphokine-mediated effector activity, these cells are associated with delayed-type hypersensitivity reactions. ( NCI )] (UMLS (CSP) C0242632) =Cell ;
72. The Read Codes Version 2
[The Read Codes Version 2 contains over 70,000 coded concepts arranged in a hierarchical structure. Top level hierarchy sections: DisordersFindings Surgical proceduresInvestigationsOccupationsDrugs ( HL7V3.0 )] (UMLS (HL7) C1553864) =Intellectual Product =CodeSystem;
23. Th2 cell
[Type 2 Helper Cells are a subset of helper-inducer T-lymphocytes which synthesize and secrete the interleukins IL-4, IL-5, IL-6, and IL-10. These cytokines influence B-cell development and antibody production as well as augmenting humoral responses. ( NCI )] (UMLS (CSP) C0242633) =Cell ;
73. The Research Foundation for Microbial Diseases of Osaka University
(UMLS (HL7) C1546875) =Health Care Related Organization =Manufacturers of Vaccines (code=MVX);
24. Thai
[Denotes the inhabitants of Thailand, a person from there, or their descendants elsewhere. ( NCI )] (UMLS (NCI) C0337910) =Population Group ;
=Asian;
74. The Research Foundation for Microbial Diseases of Osaka University (BIKEN)
[The Research Foundation for Microbial Diseases of Osaka University (BIKEN) ( HL7V3.0 )] (UMLS (HL7) C1552892) =Health Care Related Organization =VaccineManufacturer;
25. thalamic nuclei
[several groups of nuclei in the thalamus that serve as the major relay centers for sensory impulses in the brain. ( CSP )] (UMLS (CSP) C0039727) =Body Part, Organ, or Organ Component =thalamus;
75. The time post drug dose at which the highest drug level is reached (differs by drug)
(UMLS (HL7) C1547093) =Temporal Concept =Time delay post challenge;
26. thalamic radiation
[relating to the efferent connections of the thalamus with the cerebral cortex. ( CSP )] (UMLS (CSP) C0597567) =Body Part, Organ, or Organ Component ;
=central neural pathway/tract;
76. The time post drug dose at which the lowest drug level is reached (varies with drug)
(UMLS (HL7) C1547095) =Temporal Concept =Time delay post challenge;
27. Thalamostriate Vein
(UMLS (NCI) C0039728) =Body Part, Organ, or Organ Component
77. The visit is marked for deletion and the user cannot enter new data against it.
(UMLS (HL7) C1546830) =Intellectual Product =Purge Status Code;
28. thalamus
[paired bodies containing mostly gray substance and forming part of the lateral wall of the third ventricle of the brain; represents the major portion of the diencephalon. ( CSP )] (UMLS (NCI) C0039729) =Body Part, Organ, or Organ Component =diencephalon;
=conarium;
thalamic nuclei;
External Geniculate Body;
Internal Geniculate Body;
pulvinar thalami
78. The visit is marked inactive and the user cannot enter new data against it.
(UMLS (HL7) C1546831) =Intellectual Product =Purge Status Code;
29. thalassemia
[heterogeneous group of hereditary hemolytic anemias which have in common a decreased rate of synthesis of one or more hemoglobin polypeptide chains. ( CSP )] (UMLS (CSP) C0039730) =Disease or Syndrome =ANEMIA HEMOLITIKOA;
Hemoglobinopathies =Alpha Thalassemia;
Beta Thalassemia;
79. The world wide character standard from ISO/IEC 10646-1-1993
(UMLS (HL7) C1546826) =Intellectual Product =Alternate character sets;
30. thalassemia minor
[ ] (UMLS (CSP) C0085578) =Disease or Syndrome ;
80. Thebaine
[A drug that is derived from opium, which contains from 0.3-1.5% thebaine depending on its origin. It produces strychnine-like convulsions rather than narcosis. It may be habit-forming and is a controlled substance (opiate) listed in the U.S. Code of Federal Regulations, Title 21 Part 1308.12 (1985). (From Merck Index, 11th ed) ( MSH )] (UMLS (NCI) C0039746) =Organic Chemical; Pharmacologic Substance ;
31. Thalidomide/Topotecan
(UMLS (NCI) C0935811) =Therapeutic or Preventive Procedure
81. Theca Cell
[The connective tissue cells of the ovarian follicle. (MeSH) ( NCI )] (UMLS (NCI) C0039748) =Cell
32. Thalitone
(UMLS (NCI) C0700920) =Organic Chemical; Pharmacologic Substance
82. Theca Lutein Cell
[A cell of the corpus luteum that is derived from the inner layer of the sheath surrounding the graafian follicle. ( NCI )] (UMLS (NCI) C1135970) =Cell ;
33. thallium
[A heavy, soft, bluish white metal, atomic number 81, atomic weight 204.37, symbol Tl. (From Dorland, 28th ed) ( MSH )] (UMLS (CSP) C0039738) =Element, Ion, or Isotope =heavy metal;
=thallium chloride
83. Theelin
(UMLS (NCI) C1123064) =Steroid; Pharmacologic Substance; Hormone
34. thallophyte
[ ] (UMLS (CSP) C0599141) =Plant
84. Theiler's encephalomyelitis virus
[A strain of THEILOVIRUS that can be divided into two biological subgroups which both infect mice. One causes an acute and fatal polioencephalomyelitis and the other causes a chronic persistent demyelinating infection of the white matter. (7th ICTV Report, p668-9) ( MSH )] (UMLS (CSP) C0206425) =Virus
35. Tham
(UMLS (NCI) C1306531) Tham brand of tromethamine =Organic Chemical; Pharmacologic Substance
85. thematic apperception test
[A projective technique which focuses primarily on the dynamics of interpersonal relationships. It consists of a series of 31 pictures that depict various social situations and interpersonal relations. A subset is selected by the examiner and presented to the subject who is asked to tell a story about each picture. The stories are interpreted in terms of the subject's relations to authority figures, to contemporaries of both sexes, and in terms of the compromises between external demands and the needs of the id, the ego, and the superego. (From Campbell, Psychiatric Dictionary, 1996) ( MSH )] (UMLS (CSP) C0039756) =Diagnostic Procedure
36. thapsigargin
[protein kinase C independent tumor promoter; selectively inhibits Ca++/ATPase activity in the endoplasmic reticulum. ( CSP )] (UMLS (CSP) C0076374) =Organic Chemical; Hazardous or Poisonous Substance =Tumor Promoter;
86. Theo-24
(UMLS (NCI) C0700825) =Organic Chemical; Pharmacologic Substance ;
37. THBS1
[Human thrombospondin-1 protein (1170 aa, 129 kDa precursor) is encoded by the human thrombospondin-1 (THBS1) gene. This protein, a disulfide-linked homotrimer, is an adhesive extracellular matrix glycoprotein that mediates cell-to-cell and cell-to-matrix interactions. Thrombospondin-1 protein is also involved in cell migration and proliferation during embryogenesis and wound repair. It may be a regulator of tumor growth and metastasis. ( NCI )] (UMLS (NCI) C0147139) =Amino Acid, Peptide, or Protein; Biologically Active Substance
87. Theobid Duracap
(UMLS (NCI) C0700839) =Organic Chemical; Pharmacologic Substance
38. THBS1
[This gene plays a role in the mediation of both intercellular and cell-matrix interactions. It is also involved in platelet aggregation and angiogenesis. ( NCI )] (UMLS (NCI) C1336626) THBS1 Gene;
Thrombospondin 1 Gene =Gene or Genome ;
88. theobromine
[3,7-dimethylxanthine, an alkaloid found in coca with properties similar to caffeine and theophylline. ( CSP )] (UMLS (CSP) C0039763) =Organic Chemical; Pharmacologic Substance; Biologically Active Substance =alkaloid;
[CN800] CNS STIMULANTS;
Xanthine Alkaloids;
xanthine;
Muscle Relaxant;
methylpurine;
Unclassified Ingredient Preparations;
=3,7-Dihydro-3,7-dimethyl-1-(5-oxohexyl)-1H-purine-2,6-dione
39. THBS2
[Thrombospondin 2, encoded by the THBS2 gene, is a member of the thrombospondin family. Thrombospondin 2 is an adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions. It can bind to fibrinogen, fibronectin, laminin and type V collagen. It forms a disulfide-linked homotrimer. (from Swiss-Prot) ( NCI )] (UMLS (NCI) C0530678) =Amino Acid, Peptide, or Protein; Pharmacologic Substance ;
89. Theophylline Anhydrous
(UMLS (NCI) C0304441) =Organic Chemical; Pharmacologic Substance =3,7-Dihydro-1,3-dimethyl-1H-purine-2,6-dione;
[RE104] BRONCHODILATORS, XANTHINE-DERIVATIVE;
Unclassified Ingredient Preparations;
=THEOPHYLLINE,ANHYDROUS 125 MG;
THEOPHYLLINE,ANHYDROUS 300 MG;
THEOPHYLLINE,ANHYDROUS 80 MG/15ML;
THEOPHYLLINE,ANHYDROUS 200 MG;
40. THBS2
[This gene is involved in the mediation of both intercellular and cell-matrix interactions. It also plays a role in the inhibition of angiogenesis. ( NCI )] (UMLS (NCI) C1336627) THBS2 Gene;
Thrombospondin 2 Gene =Gene or Genome ;
90. Theprubicin
(UMLS (NCI) C0950476) Theprubicine =Organic Chemical; Antibiotic
41. the admitting procedure
(UMLS (HL7) C1547222) =Health Care Activity =Procedure Priority;
91. THER ULT HEAD & NECK VES
[ ] (UMLS (ICD9CM) C1135436) Therapeutic ultrasound of vessels of head and neck =Therapeutic or Preventive Procedure
42. The appointment has been confirmed; however it is confirmed in an overbooked state
(UMLS (HL7) C1548415) =Intellectual Product =Filler status codes;
92. THER ULT PERIPHERAL VES
[ ] (UMLS (ICD9CM) C1135438) Therapeutic ultrasound of peripheral vascular vessels =Therapeutic or Preventive Procedure
43. The CEN Healthcare Coding Scheme Designator. (Identifiers used in DICOM follow this assignment scheme.)
(UMLS (HL7) C1548519) =Intellectual Product =Universal ID type;
93. THER ULTRASOUND OF HEART
[ ] (UMLS (ICD9CM) C1135437) Therapeutic ultrasound of heart =Therapeutic or Preventive Procedure
44. The character set switching mode specified in HL7 2.5, section 2.7.2, _Escape sequences supporting multiple character sets_ and section 2.A.46, "XPN _ extended person name".
(UMLS (HL7) C1549934) =Idea or Concept =Alternate character set handling scheme;
94. TheraCys
(UMLS (NCI) C0307831) =Bacterium ;
45. The DCE Universal Unique Identifier
(UMLS (HL7) C1548525) =Intellectual Product =Universal ID type;
95. THERAPEU ERYTHROPHERESIS
[ ] (UMLS (ICD9CM) C0842378) Therapeutic erythrocytapheresis =Therapeutic or Preventive Procedure
46. The examining device goes to patient's location
(UMLS (HL7) C1548300) =Idea or Concept =Transportation Mode;
96. THERAPEUT DISTENT BLADD
(UMLS (ICD9CM) C0039788) =Therapeutic or Preventive Procedure
47. The first service request in a cyclic group
(UMLS (HL7) C1548964) =Idea or Concept =Cyclic Entry/Exit Indicator;
97. THERAPEUT EVAC ANT CHAMB
[ ] (UMLS (ICD9CM) C0197511) =Therapeutic or Preventive Procedure
48. the hour of sleep (e.g., H18-22)
(UMLS (HL7) C1549042) =Temporal Concept =Event related period;
98. Therapeutic
(UMLS (HL7) C1547427) =Intellectual Product =Location Service Code;
49. The indicated appointment has begun and is currently in progress
(UMLS (HL7) C1548417) =Intellectual Product =Filler status codes;
99. therapeutic
[Substitution occurred with another product having the same therapeutic objective. ( HL7V3.0 )] (UMLS (HL7) C1553525) =Health Care Activity =generic;
50. The indicated appointment has completed normally (was not discontinued, canceled, or deleted)
(UMLS (HL7) C1548411) =Intellectual Product =Filler status codes;
100. therapeutic
[Used to treat disease and help healing take place. ( NCI )] (UMLS (NCI) C0302350) =Functional Concept

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