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: 133 page 1 of 2

1. Cyst
(UMLS (HL7) C1546594) =Intellectual Product =Specimen Source Codes;
51. cystathionine
[ ] (UMLS (CSP) C0010640) =Amino Acid, Peptide, or Protein; Biologically Active Substance
2. Cyst
(UMLS (HL7) C1550626) =Body Substance =SpecimenEntityType;
52. 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
3. 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
53. 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
4. Cyst and pseudocyst of pancreas
(UMLS (ICD9CM) C0010623) =Neoplastic Process ;
54. cystathioninuria
[ ] (UMLS (CSP) C0220993) =Disease or Syndrome
5. Cyst of Endoderm
(UMLS (NCI) C1333390) Cyst of the Endoderm;
Endodermal Cyst;
Endodermal Cysts =Finding
55. 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 ;
6. 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;
56. 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
7. 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
57. 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 ;
8. Cyst of External Ear
(UMLS (NCI) C1333493) Cyst of the External Ear;
External Ear Cyst;
=Finding ;
58. 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 ;
9. Cyst of Eyelid
(UMLS (NCI) C0155218) =Finding ;
59. 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
10. Cyst of Iris
(UMLS (NCI) C0271119) =Finding ;
60. cystectomy
[surgical procedures for the excision of the urinary bladder. ( CSP )] (UMLS (CSP) C0010651) =Therapeutic or Preventive Procedure =urinary tract surgery;
11. 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;
61. 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
12. CYST OF KIDNEY, ACQUIRED
[ ] (UMLS (ICD9CM) C0268799) =Disease or Syndrome
62. 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
13. Cyst of Lacrimal Gland
(UMLS (NCI) C0271323) =Finding
63. 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 ;
14. Cyst of Liver
(UMLS (NCI) C0267834) =Disease or Syndrome ;
64. 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 ;
15. 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
65. 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 ;
16. Cyst of Meninges
(UMLS (NCI) C0347534) =Anatomical Abnormality
66. 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 ;
17. Cyst of Mouth
(UMLS (NCI) C0494710) =Acquired Abnormality ;
67. Cystic Basal Cell Carcinoma
(UMLS (NCI) C1275193) Skin Cystic Basal Cell Carcinoma =Neoplastic Process
18. Cyst of Nasal Cavity
(UMLS (NCI) C0339823) =Neoplastic Process ;
68. 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
19. 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
69. Cystic Duct Stone
(UMLS (NCI) C0267863) =Disease or Syndrome
20. 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;
70. Cystic Endometrial Hyperplasia
(UMLS (NCI) C0010673) =Neoplastic Process
21. 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
71. CYSTIC FIBROS W PUL MAN
[ ] (UMLS (ICD9CM) C0348815) =Disease or Syndrome
22. Cyst of Parathyroid
(UMLS (NCI) C0342347) =Anatomical Abnormality ;
72. CYSTIC FIBROS W/O ILEUS
(UMLS (ICD9CM) C0010676) =Disease or Syndrome
23. Cyst of Pharynx
(UMLS (NCI) C0264291) =Disease or Syndrome
73. cystic fibrosis
[most common potentially lethal autosomal recessive disease affecting Caucasians; characterized by chronic pulmonary, intestinal, liver, pancreatic, and exocrine gland dysfunction; caused by mutations of the CFTR chloride channel. ( CSP )] (UMLS (CSP) C0010674) =Disease or Syndrome =Infant, Newborn, Diseases;
Lung Diseases;
Diseases of pancreas;
inborn biological transport disorder
24. Cyst of pharynx or nasopharynx
(UMLS (ICD9CM) C0155845) =Disease or Syndrome
74. CYSTIC FIBROSIS GENE CAR
[ ] (UMLS (ICD9CM) C1135311) Cystic fibrosis gene carrier =Finding ;
25. 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
75. CYSTIC FIBROSIS NEC
[ ] (UMLS (ICD9CM) C0494350) =Disease or Syndrome
26. CYST OF PROSTATE
[ ] (UMLS (ICD9CM) C1443972) =Disease or Syndrome ;
76. CYSTIC FIBROSIS W GI MAN
(UMLS (ICD9CM) C1135187) Cystic fibrosis with gastrointestinal manifestations;
=Disease or Syndrome
27. 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
77. CYSTIC FIBROSIS W ILEUS
(UMLS (ICD9CM) C0546982) =Disease or Syndrome
28. Cyst of Scrotum
(UMLS (NCI) C0240969) =Finding
78. Cystic Hygroma
[A benign lymphatic neoplasm usually arising from the neck and characterized by cystic dilation of the lymphatic vessels. ( NCI )] (UMLS (NCI) C0206620) =Neoplastic Process ;
=lymphangioma;
29. Cyst of Spinal Arachnoid
(UMLS (NCI) C0344484) =Finding ;
79. Cystic Hygroma of Mediastinum
[A lymphangioma arising from the mediastinum. ( NCI )] (UMLS (NCI) C1334664) Cystic Hygroma of the Mediastinum;
Lymphangioma of Mediastinum;
Lymphangioma of the Mediastinum;
Mediastinal Cystic Hygroma;
Mediastinal Lymphangioma =Neoplastic Process
30. 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
80. Cystic Hypersecretory Breast Carcinoma
[A rare, low grade invasive adenocarcinoma of the breast characterized by the presence of cells that secrete milk-like material. Morphologically, it usually appears as a circumscribed lesion, composed of cystic spaces, tubular structures, and solid areas. ( NCI )] (UMLS (NCI) C0334371) =Neoplastic Process
31. Cyst of Spinal Meninges
(UMLS (NCI) C0270691) =Finding
81. CYSTIC KIDNEY DISEAS NEC
(UMLS (ICD9CM) C0431705) =Congenital Abnormality; Disease or Syndrome
32. Cyst of Testis
(UMLS (NCI) C0241351) =Finding
82. CYSTIC KIDNEY DISEAS NOS
[ ] (UMLS (ICD9CM) C0311245) =Congenital Abnormality; Disease or Syndrome ;
33. Cyst of the Thyroid
[Abnormal fluid filled sac within the thyroid gland. ( NCI )] (UMLS (NCI) C0162299) =Disease or Syndrome
83. Cystic Mesothelioma
[A peritoneal mesothelioma affecting mainly young females and producing cysts of variable size and number lined by a single layer of benign mesothelial cells. The disease follows a benign course and is compatible with a normal life expectancy, requiring occasionally partial excision or decompression for relief of pain or other symptoms. Malignant potential is exceptional. (From Holland et al., Cancer Medicine, 3d ed, p1345) ( MSH )] (UMLS (NCI) C0206680) =Neoplastic Process ;
=mesothelioma;
34. Cyst of the Urethra
(UMLS (NCI) C0268877) =Neoplastic Process
84. cystic mole
[ ] (UMLS (CSP) C0598626) =Neoplastic Process ;
35. Cyst of the Vagina
(UMLS (NCI) C0241619) =Finding
85. Cystic Neoplasm
(UMLS (NCI) C1333190) Cystic Tumor =Neoplastic Process ;
36. Cyst, Baker's
(UMLS (HL7) C1546548) =Intellectual Product =Specimen Source Codes;
86. Cystic Partially Differentiated Nephroblastoma
[A variant of Wilm tumor of the kidney characterized by the presence of cystic spaces separated by septa. The septa contain immature epithelial cells, immature stromal cells, and blastema cells. Surgical resection is usually curative. ( NCI )] (UMLS (NCI) C1266139) Malignant Cystic Nephroma;
Malignant Multilocular Cystic Nephroma =Neoplastic Process
37. Cyst, Inclusion
(UMLS (HL7) C1546670) =Intellectual Product =Specimen Source Codes;
87. Cystic Teratoma
(UMLS (NCI) C1368903) =Neoplastic Process ;
38. Cyst, Pilonidal
(UMLS (HL7) C1546736) =Intellectual Product =Specimen Source Codes;
88. Cystic Vein
(UMLS (NCI) C0226741) =Body Part, Organ, or Organ Component
39. Cyst, Renal
(UMLS (HL7) C1546765) =Intellectual Product =Specimen Source Codes;
89. CYSTICERCOSIS
[Infection with CYSTICERCUS, a larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. (From Dorland, 28th ed) ( MSH )] (UMLS (ICD9CM) C0010678) =Disease or Syndrome =Taeniasis;
=Neurocysticercosis
40. 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
90. cystine
[disulfide dimer of cysteine. ( CSP )] (UMLS (CSP) C0010682) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Biologically Active Substance =Amino Acids, Diamino;
Amino Acids, Dicarboxylic;
cysteine;
Disulfides;
Inactive Ingredient Preparations;
=CYSTINE 0.35 %;
CYSTINE 26 MG/GM;
41. Cystadenocarcinoma of Ovary
(UMLS (NCI) C1096638) Cystadenocarcinoma of the Ovary;
Ovarian Cystadenocarcinoma;
=Neoplastic Process ;
91. cystine storage disease
[lysosomal storage disorders of unknown molecular defect, characterized by widespread deposition of cystine crystals in reticuloendothelial cells. ( CSP )] (UMLS (CSP) C0010690) =Disease or Syndrome =Amino Acid Metabolism, Inborn Errors;
inborn renal tubular transport disorder =De Toni-Debre-Fanconi Syndrome
42. Cystadenocarcinoma of Pancreas
(UMLS (NCI) C0238337) =Neoplastic Process
92. cystinuria
[inherited abnormality of renal tubular transport of dibasic amino acids leading to massive urinary excretion of cystine, lysine, arginine, and ornithine. ( CSP )] (UMLS (CSP) C0010691) =Disease or Syndrome =Amino Acid Metabolism, Inborn Errors;
Aminoaciduria, Renal;
inborn renal tubular transport disorder;
avanim bedarxe hasheten kolel klayot
43. Cystadenocarcinoma of Salivary Gland
(UMLS (NCI) C1335897) Cystadenocarcinoma of the Salivary Gland;
Salivary Gland Cystadenocarcinoma;
=Neoplastic Process ;
93. cystisine
[ ] (UMLS (CSP) C0597783) =Organic Chemical ;
44. Cystadenofibroma
(UMLS (NCI) C1377849) =Neoplastic Process
94. Cystitis
[Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. ( MSH )] (UMLS (ICD9CM) C0010692) =Disease or Syndrome =Bladder Diseases;
=Cystitis, Interstitial
45. 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
95. CYSTITIS CYSTICA
(UMLS (ICD9CM) C0152262) =Disease or Syndrome ;
46. Cystadenoma of Extrahepatic Bile Duct
(UMLS (NCI) C1333504) Cystadenoma of the Extrahepatic Bile Duct;
Extrahepatic Bile Duct Cystadenoma;
=Neoplastic Process ;
96. Cystitis Glandularis
(UMLS (NCI) C0268837) =Disease or Syndrome
47. Cystadenoma of Intrahepatic Bile Duct
(UMLS (NCI) C1334257) Cystadenoma of the Intrahepatic Bile Duct;
Intrahepatic Bile Duct Cystadenoma =Neoplastic Process
97. Cystitis in diseases classified elsewhere
(UMLS (ICD9CM) C0156269) =Disease or Syndrome ;
48. Cystadenoma of Pancreas
[A non-metastasizing cystic epithelial neoplasm arising from the exocrine pancreas. ( NCI )] (UMLS (NCI) C0341486) =Neoplastic Process
98. CYSTITIS NEC
[ ] (UMLS (ICD9CM) C0029836) =Disease or Syndrome ;
49. Cystagon
(UMLS (NCI) C0733368) =Organic Chemical; Pharmacologic Substance ;
99. Cystitis/other urinary infection NOS
(UMLS (ICPC) C0497418) (Cystitis/other urinary infection NOS; ZISTITIA/BESTE GERNU ZOLDURA BAT(ESKL.E.S.T.); Cystit/anden urinvejsinfektion INA; Cystitis/urineweginfecties NAO; RAKKOTULEHDUS/VIRTSATIETULEHDUS NUD; Cystite/autre infect urinaire NP; Zystitis/Harnwegsinfektionen NNB; zihum bedarxe hasheten; cystitis/egyeb nem megh.fertozes; Cistite/altra infez urin NSA; BLAEREKAT/URINVEISINFEKSJON INA; Cistite/outra infeccao urinaria NE; Cistitis/otras inf urinarias NE; BLASKATARR/CYSTIT/OVRIGA URINVAGSINFEKTIONER UNS) Cystitis/other urin infect NOS =Disease or Syndrome =Urologic; Diagnosis/Diseases Component
50. cystathionase deficiency
[ ] (UMLS (CSP) C0268616) =Disease or Syndrome
100. CYSTO & RECTO W GRF/PROS
[ ] (UMLS (ICD9CM) C1955495) Repair of cystocele and rectocele with graft or prosthesis;
=Therapeutic or Preventive Procedure

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