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
CY CY CYA CYB CYC CYE CYF CYK CYL CYM CYP CYS CYT
selected terms: 496 page 3 of 5

201. CYP1A1
[This gene plays a role in the oxidation of procarcinogens. This process activates these compounds to carcinogens. ( NCI )] (UMLS (NCI) C0919425) CYP1A1 Gene;
Cytochrome P450, Family 1, Subfamily A, Polypeptide 1 Gene =Gene or Genome ;
251. Cyst of Pharynx
(UMLS (NCI) C0264291) =Disease or Syndrome
202. CYP1A2
[This gene plays a role in the oxidation/activation of procarcinogens. It is also involved in the metabolism of drugs and other xenobiotics. ( NCI )] (UMLS (NCI) C1332826) CYP1A2 Gene;
Cytochrome P450, Family 1, Subfamily A, Polypeptide 2 Gene =Gene or Genome
252. Cyst of pharynx or nasopharynx
(UMLS (ICD9CM) C0155845) =Disease or Syndrome
203. CYP21A2
[This gene plays a role in steroid metabolism. ( NCI )] (UMLS (NCI) C1413861) CYP21A2 Gene;
Cytochrome P450, Family 21, Subfamily A, Polypeptide 2 Gene =Gene or Genome
253. Cyst of Pineal Gland
[A fluid filled sac within the pineal gland. It is usually an incidental finding of no real clinical significance. ( NCI )] (UMLS (NCI) C1335411) Cyst of the Pineal Gland;
Pineal Cyst;
Pineal Gland Cyst =Finding
204. CYP27B1
[This gene is involved in vitamin D metabolism and calcium homeostasis. ( NCI )] (UMLS (NCI) C1413865) CYP27B1 Gene;
Cytochrome P450, Family 27, Subfamily B, Polypeptide 1 Gene =Gene or Genome
254. CYST OF PROSTATE
[ ] (UMLS (ICD9CM) C1443972) =Disease or Syndrome ;
205. CYP2A6
[This gene plays a role in the oxidation of nicotine to its carcinogenic metabolites. ( NCI )] (UMLS (NCI) C1413868) CYP2A6 Gene;
Cytochrome P450, Family 2, Subfamily A, Polypeptide 6 Gene =Gene or Genome
255. Cyst of Rathke's Pouch
[Rathke's pouch cysts are rarely symptomatic in the first two decades of life though they may produce symptoms in the third and fourth decades of life. When the cysts do present in the first decades of life, the symptoms are generally associated with diabetes insipidus or other conditions related to hypopituitarism. ( NCI )] (UMLS (NCI) C0752244) Rathke Cleft Cyst;
Rathke Pouch Cyst;
Rathke's Pouch Cyst;
Suprasellar Cyst =Congenital Abnormality; Disease or Syndrome
206. CYP2B6
[This gene is involved in the oxidation of both endogenous substrates and drugs/xenobiotics. ( NCI )] (UMLS (NCI) C1382176) CYP2B6 Gene;
Cytochrome P450, Family 2, Subfamily B, Polypeptide 6 Gene =Gene or Genome
256. Cyst of Scrotum
(UMLS (NCI) C0240969) =Finding
207. CYP2C18
[This gene plays a role in the metabolism of fatty acids, tryptophan, drugs and xenobiotics. ( NCI )] (UMLS (NCI) C1378702) CYP2C18 Gene;
Cytochrome P450, Family 2, Subfamily C, Polypeptide 18 Gene;
=Gene or Genome
257. Cyst of Spinal Arachnoid
(UMLS (NCI) C0344484) =Finding ;
208. CYP2C19
[This gene is involved in the metabolism of drugs and xenobiotics. ( NCI )] (UMLS (NCI) C1332828) CYP2C19 Gene;
Cytochrome P450, Family 2, Subfamily C, Polypeptide 19 Gene =Gene or Genome
258. Cyst of Spinal Canal and Spinal Cord
(UMLS (NCI) C1334263) Cyst of the Spinal Canal and Spinal Cord;
Intraspinal Cyst;
Intraspinal Cysts;
Spinal Canal and Spinal Cord Cyst =Finding
209. CYP2C8
[This gene plays a role in drug metabolism. It is also involved in the oxidation of both endobiotics and xenobiotics. ( NCI )] (UMLS (NCI) C1413873) CYP2C8 Gene;
Cytochrome P450, Family 2, Subfamily C, Polypeptide 8 Gene =Gene or Genome
259. Cyst of Spinal Meninges
(UMLS (NCI) C0270691) =Finding
210. CYP2C9
[This gene is involved in the oxidation of drugs, xenobiotics, fatty acids and steroids. ( NCI )] (UMLS (NCI) C1332829) CYP2C9 Gene;
Cytochrome P450, Family 2, Subfamily C, Polypeptide 9 Gene =Gene or Genome
260. Cyst of Testis
(UMLS (NCI) C0241351) =Finding
211. CYP2D5
[Cytochrome P450 2D5 is a rat liver ER membrane-bound heme-thiolate monooxygenase, involved in an NADPH-dependent electron transport pathway that oxidizes various compounds, including steroids, fatty acids, and xenobiotics. Expression is induced in liver and other tissues by drugs, pesticides, and carcinogens. ( NCI )] (UMLS (NCI) C1333193) Cytochrome P450 2D5 =Amino Acid, Peptide, or Protein; Enzyme
261. Cyst of the Thyroid
[Abnormal fluid filled sac within the thyroid gland. ( NCI )] (UMLS (NCI) C0162299) =Disease or Syndrome
212. CYP2D6
[This gene plays a role in the metabolism of numerous clinically-relevant drugs. It is also involved in the oxidation of xenobiotics. ( NCI )] (UMLS (NCI) C1332830) CYP2D6 Gene;
Cytochrome P450, Family 2, Subfamily D, Polypeptide 6 Gene =Gene or Genome
262. Cyst of the Urethra
(UMLS (NCI) C0268877) =Neoplastic Process
213. CYP2E1
[This gene is involved in the metabolism of both endogenous and exogenous substrates. ( NCI )] (UMLS (NCI) C0919426) CYP2E1 Gene;
Cytochrome P450, Family 2, Subfamily E, Polypeptide 1 Gene =Gene or Genome ;
263. Cyst of the Vagina
(UMLS (NCI) C0241619) =Finding
214. CYP3A4
[Induced primarily in liver by glucocorticoids, drugs, pesticides, and carcinogens and encoded by human CYP3A4 Gene (Cytochrome P450 IIIA Subfamily), Cytochrome P450 3A4 is a 502-amino acid 57.3-kD membrane-bound ER heme-thiolate monooxygenase. CYP3A4 is involved in an NADPH-dependent electron transport pathway and phase I oxidative metabolism of carcinogens, steroids, fatty acids, and xenobiotics, as well as bioactivation of aflatoxin B(1) to a genotoxic derivative. Activity seems a key predictor of drug responsiveness and toxicity. (from LocusLink, Swiss-Prot, OMIM, and NCI) ( NCI )] (UMLS (NCI) C1142644) Cytochrome P450 3A4;
Cytochrome P450 Nifedipine Oxidase;
Cytochrome P450, Subfamily IIIA (Niphedipine Oxidase), Polypeptide 3;
Cytochrome P450, Subfamily IIIA (Niphedipine Oxidase), Polypeptide 4;
Cytochrome P450, Subfamily IIIA, Polypeptide 4;
Cytochrome P450PCN1;
EC 1.14.14.1;
Glucocorticoid-Inducible P450;
Nifedipine Oxidase;
P450, FAMILY III;
P450-3A4;
P450-III, Steroid Inducible;
P450-III, Steroid-Inducible;
Quinine 3-Monooxygenase;
Steroid-Inducible P450- III =Amino Acid, Peptide, or Protein; Enzyme
264. Cyst, Baker's
(UMLS (HL7) C1546548) =Intellectual Product =Specimen Source Codes;
215. CYP3A4
[This gene plays an role in the metabolism of numerous clinically-relevant drugs. It is also involved in the oxidation of both endogenous substrates and xenobiotics. ( NCI )] (UMLS (NCI) C1176140) CYP3A4 Gene;
Cytochrome P450, Family 3, Subfamily A, Polypeptide 4 Gene =Gene or Genome ;
265. Cyst, Inclusion
(UMLS (HL7) C1546670) =Intellectual Product =Specimen Source Codes;
216. CYP3A5
[This gene is involved in the metabolism of fatty acids, steroids, drugs and xenobiotics. It also plays a role in the metabolism of sex hormones. ( NCI )] (UMLS (NCI) C1413882) CYP3A5 Gene;
Cytochrome P450, Family 3, Subfamily A, Polypeptide 5 Gene =Gene or Genome
266. Cyst, Pilonidal
(UMLS (HL7) C1546736) =Intellectual Product =Specimen Source Codes;
217. CYP3A7
[This gene plays a role in the metabolism of drugs, xenobiotics, fatty acids and steroids. It is also involved in the synthesis of estriol during pregnancy. ( NCI )] (UMLS (NCI) C1413884) CYP3A7 Gene;
Cytochrome P450, Family 3, Subfamily A, Polypeptide 7 Gene =Gene or Genome
267. Cyst, Renal
(UMLS (HL7) C1546765) =Intellectual Product =Specimen Source Codes;
218. CYP7A1
[This gene is involved in bile acid synthesis and steroid metabolism. ( NCI )] (UMLS (NCI) C1413893) CYP7A1 Gene;
Cytochrome P450, Family 7, Subfamily A, Polypeptide 1 Gene =Gene or Genome
268. Cystadenocarcinoma
[A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and invasiveness, and local extension and metastases occur. Cystadenocarcinomas develop frequently in the ovaries, where pseudomucinous and serous types are recognized. (Stedman, 25th ed) ( MSH )] (UMLS (NCI) C0010631) =Neoplastic Process ;
=adenocarcinoma;
Neoplasms, Cystic, Mucinous, and Serous =Cystadenocarcinoma, Mucinous;
Cystadenocarcinoma, Papillary;
Cystadenocarcinoma, Serous
219. CYP8B1
[This gene plays a role in steroid metabolism and regulation of cholesterol solubility. ( NCI )] (UMLS (NCI) C1413895) CYP8B1 Gene;
Cytochrome P450, Family 8, Subfamily B, Polypeptide 1 Gene =Gene or Genome
269. Cystadenocarcinoma of Ovary
(UMLS (NCI) C1096638) Cystadenocarcinoma of the Ovary;
Ovarian Cystadenocarcinoma;
=Neoplastic Process ;
220. CyPat
(UMLS (NCI) C0919249) =Steroid; Pharmacologic Substance ;
270. Cystadenocarcinoma of Pancreas
(UMLS (NCI) C0238337) =Neoplastic Process
221. Cypovirus
[isolated from arthropods; virions occluded within proteinaceous occlusion bodies (polyhedra); 12 virus types have been identified. ( CSP )] (UMLS (CSP) C1148555) =Virus =Reoviridae;
271. Cystadenocarcinoma of Salivary Gland
(UMLS (NCI) C1335897) Cystadenocarcinoma of the Salivary Gland;
Salivary Gland Cystadenocarcinoma;
=Neoplastic Process ;
222. Cypridina luciferin 2 monooxygenase
[ ] (UMLS (CSP) C0311726) =Amino Acid, Peptide, or Protein; Enzyme
272. Cystadenofibroma
(UMLS (NCI) C1377849) =Neoplastic Process
223. Cyprinidae
[any of various freshwater fish of the family Cyprinidae. ( CSP )] (UMLS (CSP) C0010613) =Fish ;
=bony fish;
=Carassius auratus;
Brachydanio rerio;
273. Cystadenoma
[A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) ( MSH )] (UMLS (NCI) C0010633) =Neoplastic Process ;
=adenoma;
Neoplasms, Cystic, Mucinous, and Serous =Cystadenoma, Mucinous;
Cystadenoma, Papillary;
Cystadenoma, Serous
224. Cyprinus
[Genus containing one species (Cyprinus carpio), in the family CYPRINIDAE. ( MSH )] (UMLS (CSP) C0086083) =Fish
274. Cystadenoma of Extrahepatic Bile Duct
(UMLS (NCI) C1333504) Cystadenoma of the Extrahepatic Bile Duct;
Extrahepatic Bile Duct Cystadenoma;
=Neoplastic Process ;
225. cyproheptadine
[serotonin antagonist and histamine H1 blocker used as an antipruritic, appetite stimulant, antiallergic, and to treat the post-gastrectomy dumping syndrome. ( CSP )] (UMLS (CSP) C0010620) =Organic Chemical; Pharmacologic Substance =[AH000] ANTIHISTAMINES;
Dibenzocycloheptenes;
Piperidines;
cycloheptane;
[AH700] ANTIHISTAMINES, PIPERIDINE;
=azatadine;
LORATADINE;
CYPROHEPTADINE HYDROCHLORIDE
275. Cystadenoma of Intrahepatic Bile Duct
(UMLS (NCI) C1334257) Cystadenoma of the Intrahepatic Bile Duct;
Intrahepatic Bile Duct Cystadenoma =Neoplastic Process
226. cyproterone
[A synthetic steroidal anti-androgen with antineoplastic activity. Cyproterone, in its acetate form, binds the androgen receptor (AR), thereby preventing androgen-induced receptor activation and inhibiting the growth of testosterone-sensitive tumor cells. This agent also exerts progesterogenic activity, resulting in a reduction in testicular androgen secretion and total androgen blockade. (NCI04) ( NCI )] (UMLS (CSP) C0010621) =Steroid; Pharmacologic Substance
276. Cystadenoma of Pancreas
[A non-metastasizing cystic epithelial neoplasm arising from the exocrine pancreas. ( NCI )] (UMLS (NCI) C0341486) =Neoplastic Process
227. Cyproterone/Leuprolide
(UMLS (NCI) C1327832) =Therapeutic or Preventive Procedure ;
277. Cystagon
(UMLS (NCI) C0733368) =Organic Chemical; Pharmacologic Substance ;
228. Cyproterone/Triptorelin
(UMLS (NCI) C1327903) =Therapeutic or Preventive Procedure ;
278. cystathionase deficiency
[ ] (UMLS (CSP) C0268616) =Disease or Syndrome
229. Cyst
(UMLS (HL7) C1546594) =Intellectual Product =Specimen Source Codes;
279. cystathionine
[ ] (UMLS (CSP) C0010640) =Amino Acid, Peptide, or Protein; Biologically Active Substance
230. Cyst
(UMLS (HL7) C1550626) =Body Substance =SpecimenEntityType;
280. cystathionine gamma lyase
[A multifunctional pyridoxal phosphate enzyme. In the final step in the biosynthesis of cysteine it catalyzes the cleavage of cystathionine to yield cysteine, ammonia, and 2-ketobutyrate. EC 4.4.1.1. ( MSH )] (UMLS (CSP) C0010642) =Amino Acid, Peptide, or Protein; Enzyme
231. cyst
[(sist) A sac or capsule filled with fluid. ( NCI )] (UMLS (NCI) C0010709) =Anatomical Abnormality =KASVAIMET;
=Bone Cyst;
BRANCHIAL CLEFT CYST;
Bronchogenic Cyst;
CHALAZION;
Choledochal Cyst;
Dermoid;
ATEROM;
Cyst of Esophagus;
Breast Fibrocystic Change;
Follicular Cyst;
Cyst of Kidney;
Lymphocele;
Cystoid Macular Edema;
Cyst of Mediastinum;
Mesenteric Cyst;
Mucocele;
Mucocele of salivary gland;
Cyst of Ovary;
Cyst of Pancreas;
Parovarian Cyst;
Pilonidal cyst;
Cisti del dotto tireoglosso;
Urachal Cyst;
Arachnoid Cyst;
Synovial Cyst
281. cystathionine synthase deficiency
[autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of cystathionine beta-synthase and associated with elevations of homocysteine in plasma and urine; clinical features include a tall, slender habitus, scoliosis, arachnodactyly, muscle weakness, genu varis, thin blond hair, malar flush, lens dislocations, an increased incidence of mental retardation, and a tendency to develop fibrosis of arteries, frequently complicated by cerebrovascular accidents and myocardial infarction. ( CSP )] (UMLS (CSP) C0019880) =Disease or Syndrome ;
=Amino Acid Metabolism, Inborn Errors;
Connective Tissue Disease;
Arrieration mentale;
enzyme deficiency
232. Cyst and pseudocyst of pancreas
(UMLS (ICD9CM) C0010623) =Neoplastic Process ;
282. cystathioninuria
[ ] (UMLS (CSP) C0220993) =Disease or Syndrome
233. Cyst of Endoderm
(UMLS (NCI) C1333390) Cyst of the Endoderm;
Endodermal Cyst;
Endodermal Cysts =Finding
283. cystatin
[A homologous group of endogenous cysteine proteinase inhibitors. Four distinct families are recognized within the cystatin superfamily: cystatin B or stefins; cystatin C or post-gamma-globulin; egg-white or chicken cystatin; and kininogen cystatin. The cystatins inhibit most Cysteine Endopeptidases of the papain type, and other peptidases which have a sulfhydryl group at the active site. ( MSH )] (UMLS (CSP) C0010646) =Amino Acid, Peptide, or Protein; Pharmacologic Substance ;
234. Cyst of Epididymis
[A cystic dilation of the EPIDIDYMIS, usually in the head portion (caput epididymis). The cyst fluid contains dead SPERMATOZOA and can be easily differentiated from TESTICULAR HYDROCELE and other testicular lesions. ( MSH )] (UMLS (NCI) C0037859) =Acquired Abnormality; Disease or Syndrome =DISEASES OF MALE GENITAL ORGANS;
284. Cystatin 1 Family Gene
[One of three inhibitory families in the cystatin superfamily (including type 2 cystatins and kininogens), Stefin Family Genes (type 1 cystatins) encode intracellular cysteine thiol protease inhibitors of papain and cathepsins B, H, and L. Cystatin Superfamily proteins contain multiple cystatin-like sequences; some are active cysteine protease inhibitors, while others have lost or perhaps never acquired this activity. (NCI) ( NCI )] (UMLS (NCI) C1336499) Stefin Family Gene =Gene or Genome
235. Cyst of Esophagus
[Any fluid-filled closed cavity or sac (CYSTS) that is lined by an EPITHELIUM and found in the ESOPHAGUS region. ( MSH )] (UMLS (NCI) C0014851) =Congenital Abnormality ;
=cyst;
Disease of esophagus
285. Cystatin 2 Family Gene
[Cystatin Family Genes encode (Type 2) Cystatin proteins, secreted, tight, reversible, competitive inhibitors of cysteine proteinases that contain multiple cystatin-like sequences and have 2 intrachain disulfide bonds. Cystatin Superfamily Genes comprise three subfamilies that display structural and/or functional similarities: Stefins (Type 1 Cystatins), Cystatins (Type 2 Cystatins), and Kininogens. Some members are active cysteine protease inhibitors; others have lost or never acquired inhibitory activity. (NCI) ( NCI )] (UMLS (NCI) C1333185) Cystatin Family Gene =Gene or Genome ;
236. Cyst of External Ear
(UMLS (NCI) C1333493) Cyst of the External Ear;
External Ear Cyst;
=Finding ;
286. Cystatin Superfamily Gene
[Cystatin Superfamily Genes comprise a single evolutionary superfamily that encode protein subfamilies with functional and structural similarities that include cystatin-like sequences: Stefins (Type 1 Cystatins), Cystatins (Type 2 Cystatins), and Kininogens. Some members are active cysteine protease inhibitors; others have lost or never acquired inhibitory activity. Cystatins are intracellular or extracellular, tight, reversible, competitive inhibitors of lysosomal cysteine proteinases, such as Cathepsins B, L, H, and S, that appear to provide a protective function. Type 1 Cystatins lack disulfide bridges. Type 2 Cystatins are secreted and have 2 intrachain disulfide bonds. Kininogens contain 3 cystatin-like domains, each with 2 disulfide bonds. (NCI) ( NCI )] (UMLS (NCI) C1333186) =Gene or Genome ;
237. Cyst of Eyelid
(UMLS (NCI) C0155218) =Finding ;
287. cysteamine
[radiation protective agent that oxidizes in air to form cystamine; can be given intravenously or orally to treat radiation sickness; the bitartrate has been used for the oral treatment of nephropathic cystinosis. ( CSP )] (UMLS (CSP) C0010648) =Organic Chemical; Pharmacologic Substance ;
=Mercaptoethylamines;
Radiation Effect Modifiers;
aminothiol;
[GU900] GENITOURINARY AGENTS, OTHER;
[XX000] MISCELLANEOUS AGENTS;
=CYSTEAMINE BITARTRATE
238. Cyst of Iris
(UMLS (NCI) C0271119) =Finding ;
288. cystectomy
[surgical procedures for the excision of the urinary bladder. ( CSP )] (UMLS (CSP) C0010651) =Therapeutic or Preventive Procedure =urinary tract surgery;
239. Cyst of Kidney
[kidney containing one or more cysts, including polycystic disease, solitary cyst, multiple simple cysts, and retention cysts. ( CSP )] (UMLS (NCI) C0022679) =Disease or Syndrome =cyst;
Kidney Disease =polycystic kidney;
Kidney, Sponge;
Multicystic Dysplastic Kidney;
289. cysteine
[primary aminoacid with the side group -CH2SH, capable of forming disulfide bonds (cystine) with other cysteine residues to stabilize protein tertiary and oligomeric structure. ( CSP )] (UMLS (CSP) C0010654) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
=Amino Acids, Sulfur;
mercaptan;
Amino Acids, Neutral;
primary aminoacid;
Inactive Ingredient Preparations;
=cystine;
acetylcysteine;
cystine;
CYSTEINE HYDROCHLORIDE;
CYSTEINE HYDROCHLORIDE MONOHYDRATE;
CYSTEINE HYDROCHLORIDE;
CYSTEINE 20 MG/100ML;
CYSTEINE
240. CYST OF KIDNEY, ACQUIRED
[ ] (UMLS (ICD9CM) C0268799) =Disease or Syndrome
290. Cysteine Metabolism
[The chemical reactions and pathways involving cysteine, 2-amino-3-mercaptopropanoic acid. [GOC:go_curators] ( GO )] (UMLS (NCI) C1156850) Cysteine Metabolism Pathway;
=Molecular Function
241. Cyst of Lacrimal Gland
(UMLS (NCI) C0271323) =Finding
291. Cysteine Protease Gene
[Cysteine Protease Genes encode endopeptidases, inactivated by sulfhydryl reagents, that have a cysteine residue involved in the catalytic process. (NCI) ( NCI )] (UMLS (NCI) C1333187) Thiol Protease Gene =Gene or Genome ;
242. Cyst of Liver
(UMLS (NCI) C0267834) =Disease or Syndrome ;
292. Cysteine Proteinase Inhibitor Gene
[Human Cysteine Proteinase Inhibitor Genes encode Cysteine Proteinase Inhibitors, endogenous proteins that hinder the function of cysteine proteinases. ( NCI )] (UMLS (NCI) C1333188) =Gene or Genome ;
243. Cyst of Mediastinum
[Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus. ( MSH )] (UMLS (NCI) C0025060) =Acquired Abnormality ;
=cyst;
Mediastinal Disease
293. Cysteine-Rich Domain Associated With Ring and TRAF Domains
[The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. This protein has been shown to interact with neurotrophin receptor, p75 (NTR/NTSR1), and negatively regulate NTR induced cell death and NF-kappa B activation. This protein has been found to bind to p47phox, a cytosolic regulatory factor included in a multi-protein complex known as NAD(P)H oxidase. This protein thus, is thought to be involved in the oxidative activation of MAPK8/JNK. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. (LocusLink) ( NCI )] (UMLS (NCI) C0383122) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
244. Cyst of Meninges
(UMLS (NCI) C0347534) =Anatomical Abnormality
294. Cysteine-Rich Protein TTG-2
[Rhombotin 2, an LMO (LIM-only) family member that functions in hematopoiesis, is encoded by the LMO2 gene. With two LIM domains and a cysteine-rich motif, rhombotin 2 is part of a multi-protein transcription regulatory complex that includes GATA-1. LMO2 protein binds to the bHLH TAL1 protein and interacts with retinoblastoma binding protein-2, enhancing transcription. Chromosomal translocations involving LMO2 are associated with T-cell leukemias. (from OMIM 180385 and NCI) ( NCI )] (UMLS (NCI) C0250437) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
245. Cyst of Mouth
(UMLS (NCI) C0494710) =Acquired Abnormality ;
295. Cystic Basal Cell Carcinoma
(UMLS (NCI) C1275193) Skin Cystic Basal Cell Carcinoma =Neoplastic Process
246. Cyst of Nasal Cavity
(UMLS (NCI) C0339823) =Neoplastic Process ;
296. cystic duct
[The duct that is connected to the GALLBLADDER and allows the emptying of bile into the COMMON BILE DUCT. ( MSH )] (UMLS (CSP) C0010672) =Body Part, Organ, or Organ Component
247. Cyst of Nerve Root
[Perineurial cysts commonly found in the SACRAL REGION. They arise from the PERINEURIUM membrane within the SPINAL NERVE ROOTS. The distinctive feature of the cysts is the presence of spinal nerve root fibers within the cyst wall, or the cyst cavity itself. ( MSH )] (UMLS (NCI) C0520720) =Neoplastic Process
297. Cystic Duct Stone
(UMLS (NCI) C0267863) =Disease or Syndrome
248. Cyst of Ovary
[fluid-filled closed cavity or sac in the ovary that is lined by epithelium; can be of normal, abnormal, non-neoplastic, or neoplastic tissues. ( CSP )] (UMLS (NCI) C0029927) =Disease or Syndrome =cyst;
ovarian disease =PCOS;
298. Cystic Endometrial Hyperplasia
(UMLS (NCI) C0010673) =Neoplastic Process
249. Cyst of Pancreas
[A true cyst of the PANCREAS, distinguished from the much more common PANCREATIC PSEUDOCYST by possessing a lining of mucous EPITHELIUM. Pancreatic cysts are categorized as congenital, retention, neoplastic, parasitic, enterogenous, or dermoid. Congenital cysts occur more frequently as solitary cysts but may be multiple. Retention cysts are gross enlargements of PANCREATIC DUCTS secondary to ductal obstruction. (From Bockus Gastroenterology, 4th ed, p4145) ( MSH )] (UMLS (NCI) C0030283) =Disease or Syndrome ;
=cyst;
Diseases of pancreas =Pancreatic Pseudocyst
299. CYSTIC FIBROS W PUL MAN
[ ] (UMLS (ICD9CM) C0348815) =Disease or Syndrome
250. Cyst of Parathyroid
(UMLS (NCI) C0342347) =Anatomical Abnormality ;
300. CYSTIC FIBROS W/O ILEUS
(UMLS (ICD9CM) C0010676) =Disease or Syndrome

Buy website

Medical Clinic. Optician. Pharmacy. Physician. Travel Agency. Hotel reservation. Child Care. Education. Teachers. Lessons. Tests and Exams. Certification. Shopping Center. Store. Real Estate.
Affordable prices from $100.

 home Dictionaries Armenian-English English-Armenian MeSH Feedback  top
© 2008 -2011 Administrator MEDINDEX.AM