- 8501. 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;
| - 8551. Cystic Endometrial Hyperplasia
- (UMLS (NCI) C0010673) =Neoplastic Process
|
- 8502. 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 | - 8552. CYSTIC FIBROS W PUL MAN
- [ ] (UMLS (ICD9CM) C0348815) =Disease or Syndrome
|
- 8503. Cyst of Parathyroid
- (UMLS (NCI) C0342347) =Anatomical Abnormality ;
| - 8553. CYSTIC FIBROS W/O ILEUS
- (UMLS (ICD9CM) C0010676) =Disease or Syndrome
|
- 8504. Cyst of Pharynx
- (UMLS (NCI) C0264291) =Disease or Syndrome
| - 8554. 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 |
- 8505. Cyst of pharynx or nasopharynx
- (UMLS (ICD9CM) C0155845) =Disease or Syndrome
| - 8555. CYSTIC FIBROSIS GENE CAR
- [ ] (UMLS (ICD9CM) C1135311) Cystic fibrosis gene carrier =Finding ;
|
- 8506. 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 | - 8556. CYSTIC FIBROSIS NEC
- [ ] (UMLS (ICD9CM) C0494350) =Disease or Syndrome
|
- 8507. CYST OF PROSTATE
- [ ] (UMLS (ICD9CM) C1443972) =Disease or Syndrome ;
| - 8557. CYSTIC FIBROSIS W GI MAN
- (UMLS (ICD9CM) C1135187) Cystic fibrosis with gastrointestinal manifestations;
=Disease or Syndrome |
- 8508. 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 | - 8558. CYSTIC FIBROSIS W ILEUS
- (UMLS (ICD9CM) C0546982) =Disease or Syndrome
|
- 8509. Cyst of Scrotum
- (UMLS (NCI) C0240969) =Finding
| - 8559. 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;
|
- 8510. Cyst of Spinal Arachnoid
- (UMLS (NCI) C0344484) =Finding ;
| - 8560. 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 |
- 8511. 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 | - 8561. 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
|
- 8512. Cyst of Spinal Meninges
- (UMLS (NCI) C0270691) =Finding
| - 8562. CYSTIC KIDNEY DISEAS NEC
- (UMLS (ICD9CM) C0431705) =Congenital Abnormality; Disease or Syndrome
|
- 8513. Cyst of Testis
- (UMLS (NCI) C0241351) =Finding
| - 8563. CYSTIC KIDNEY DISEAS NOS
- [ ] (UMLS (ICD9CM) C0311245) =Congenital Abnormality; Disease or Syndrome ;
|
- 8514. Cyst of the Thyroid
- [Abnormal fluid filled sac within the thyroid gland. ( NCI )] (UMLS (NCI) C0162299) =Disease or Syndrome
| - 8564. 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;
|
- 8515. Cyst of the Urethra
- (UMLS (NCI) C0268877) =Neoplastic Process
| - 8565. cystic mole
- [ ] (UMLS (CSP) C0598626) =Neoplastic Process ;
|
- 8516. Cyst of the Vagina
- (UMLS (NCI) C0241619) =Finding
| - 8566. Cystic Neoplasm
- (UMLS (NCI) C1333190) Cystic Tumor =Neoplastic Process ;
|
- 8517. Cyst, Baker's
- (UMLS (HL7) C1546548) =Intellectual Product =Specimen Source Codes;
| - 8567. 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 |
- 8518. Cyst, Inclusion
- (UMLS (HL7) C1546670) =Intellectual Product =Specimen Source Codes;
| - 8568. Cystic Teratoma
- (UMLS (NCI) C1368903) =Neoplastic Process ;
|
- 8519. Cyst, Pilonidal
- (UMLS (HL7) C1546736) =Intellectual Product =Specimen Source Codes;
| - 8569. Cystic Vein
- (UMLS (NCI) C0226741) =Body Part, Organ, or Organ Component
|
- 8520. Cyst, Renal
- (UMLS (HL7) C1546765) =Intellectual Product =Specimen Source Codes;
| - 8570. 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 |
- 8521. 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 | - 8571. 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;
|
- 8522. Cystadenocarcinoma of Ovary
- (UMLS (NCI) C1096638) Cystadenocarcinoma of the Ovary;
Ovarian Cystadenocarcinoma;
=Neoplastic Process ;
| - 8572. 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 |
- 8523. Cystadenocarcinoma of Pancreas
- (UMLS (NCI) C0238337) =Neoplastic Process
| - 8573. 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 |
- 8524. Cystadenocarcinoma of Salivary Gland
- (UMLS (NCI) C1335897) Cystadenocarcinoma of the Salivary Gland;
Salivary Gland Cystadenocarcinoma;
=Neoplastic Process ;
| - 8574. cystisine
- [ ] (UMLS (CSP) C0597783) =Organic Chemical ;
|
- 8525. Cystadenofibroma
- (UMLS (NCI) C1377849) =Neoplastic Process
| - 8575. 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 |
- 8526. 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 | - 8576. CYSTITIS CYSTICA
- (UMLS (ICD9CM) C0152262) =Disease or Syndrome ;
|
- 8527. Cystadenoma of Extrahepatic Bile Duct
- (UMLS (NCI) C1333504) Cystadenoma of the Extrahepatic Bile Duct;
Extrahepatic Bile Duct Cystadenoma;
=Neoplastic Process ;
| - 8577. Cystitis Glandularis
- (UMLS (NCI) C0268837) =Disease or Syndrome
|
- 8528. Cystadenoma of Intrahepatic Bile Duct
- (UMLS (NCI) C1334257) Cystadenoma of the Intrahepatic Bile Duct;
Intrahepatic Bile Duct Cystadenoma =Neoplastic Process | - 8578. Cystitis in diseases classified elsewhere
- (UMLS (ICD9CM) C0156269) =Disease or Syndrome ;
|
- 8529. Cystadenoma of Pancreas
- [A non-metastasizing cystic epithelial neoplasm arising from the exocrine pancreas. ( NCI )] (UMLS (NCI) C0341486) =Neoplastic Process
| - 8579. CYSTITIS NEC
- [ ] (UMLS (ICD9CM) C0029836) =Disease or Syndrome ;
|
- 8530. Cystagon
- (UMLS (NCI) C0733368) =Organic Chemical; Pharmacologic Substance ;
| - 8580. 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
|
- 8531. cystathionase deficiency
- [ ] (UMLS (CSP) C0268616) =Disease or Syndrome
| - 8581. CYSTO & RECTO W GRF/PROS
- [ ] (UMLS (ICD9CM) C1955495) Repair of cystocele and rectocele with graft or prosthesis;
=Therapeutic or Preventive Procedure |
- 8532. cystathionine
- [ ] (UMLS (CSP) C0010640) =Amino Acid, Peptide, or Protein; Biologically Active Substance
| - 8582. CYSTOCEL/RECTOCEL REPAIR
- (UMLS (ICD9CM) C0195232) =Therapeutic or Preventive Procedure
|
- 8533. 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
| - 8583. cystocele
- [A HERNIA-like condition in which the weakened pelvic muscles cause the URINARY BLADDER to drop from its normal position. Fallen urinary bladder is more common in females with the bladder dropping into the VAGINA and less common in males with the bladder dropping into the SCROTUM. ( MSH )] (UMLS (CSP) C0010695) =Acquired Abnormality; Disease or Syndrome ;
|
- 8534. 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 | - 8584. CYSTOCELE REPAIR
- [ ] (UMLS (ICD9CM) C1261300) Repair of cystocele =Therapeutic or Preventive Procedure
|
- 8535. cystathioninuria
- [ ] (UMLS (CSP) C0220993) =Disease or Syndrome
| - 8585. CYSTOCELE, LATERAL
- [ ] (UMLS (ICD9CM) C1456249) =Disease or Syndrome
|
- 8536. 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 ;
| - 8586. CYSTOCELE, MIDLINE
- [ ] (UMLS (ICD9CM) C1456248) =Acquired Abnormality; Disease or Syndrome
|
- 8537. 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
| - 8587. Cystogenic Ameloblastoma
- (UMLS (NCI) C0457521) =Neoplastic Process
|
- 8538. 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 ;
| - 8588. CYSTOGRAM NEC
- [ ] (UMLS (ICD9CM) C0177747) =Diagnostic Procedure
|
- 8539. 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 ;
| - 8589. Cystography
- [A radiographic procedure to obtain an image of the urinary bladder by filling the bladder with contrast medium. ( NCI )] (UMLS (NCI) C0203126) =Diagnostic Procedure
|
- 8540. 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 | - 8590. CYSTOID MACULAR DEGEN
- [ ] (UMLS (ICD9CM) C0154850) =Disease or Syndrome
|
- 8541. cystectomy
- [surgical procedures for the excision of the urinary bladder. ( CSP )] (UMLS (CSP) C0010651) =Therapeutic or Preventive Procedure =urinary tract surgery;
| - 8591. Cystoid Macular Edema
- [Fluid accumulation in the outer layer of the MACULA LUTEA at the center of the RETINA in a petaloid pattern where cystic spaces are formed and may lead to macular depressions or holes. ( MSH )] (UMLS (NCI) C0024440) =Disease or Syndrome ;
=cyst;
Degeneracion macular |
- 8542. 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 | - 8592. CYSTOMETROGRAM
- [ ] (UMLS (ICD9CM) C0200000) =Diagnostic Procedure
|
- 8543. 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 | - 8593. Cystoprostatectomy
- (UMLS (NCI) C0194412) =Therapeutic or Preventive Procedure
|
- 8544. 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 ;
| - 8594. cystosarcoma phyllodes
- [A type of connective tissue neoplasm arising from intralobular stroma of the BREAST. It is characterized by the rapid enlargement of an asymmetric firm mobile mass. Histologically, its leaf-like stromal clefts are lined by EPITHELIAL CELLS. ( MSH )] (UMLS (NCI) C0010701) =Neoplastic Process =Fibroadenoma;
Connective Tissue Sarcoma;
breast neoplasm;
|
- 8545. 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 ;
| - 8595. Cystosarcoma Phyllodes of Prostate
- (UMLS (NCI) C1335409) Cystosarcoma Phyllodes of the Prostate;
Phyllodes Neoplasm of Prostate;
Phyllodes Neoplasm of the Prostate;
Phyllodes Tumor of Prostate;
Phyllodes Tumor of the Prostate;
Prostate Cystosarcoma Phyllodes;
Prostate Phyllodes Neoplasm;
Prostate Phyllodes Tumor;
=Neoplastic Process |
- 8546. 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 ;
| - 8596. cystoscope
- [(SIS-toe-skope) A thin, lighted instrument used to look inside the bladder and remove tissue samples or small tumors. ( NCI )] (UMLS (NCI) C0180274) =Medical Device
|
- 8547. 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 ;
| - 8597. cystoscopy
- [endoscopic examination, therapy or surgery of the urinary bladder. ( CSP )] (UMLS (CSP) C0010702) =Diagnostic Procedure =Endoscopic;
urinary tract imaging/visualization;
Modality;
|
- 8548. Cystic Basal Cell Carcinoma
- (UMLS (NCI) C1275193) Skin Cystic Basal Cell Carcinoma =Neoplastic Process
| - 8598. CYSTOSCOPY NEC
- [ ] (UMLS (ICD9CM) C0029568) =Diagnostic Procedure ;
|
- 8549. 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
| - 8599. Cystoscopy through artificial stoma
- [ ] (UMLS (ICD9CM) C0177030) =Diagnostic Procedure
|
- 8550. Cystic Duct Stone
- (UMLS (NCI) C0267863) =Disease or Syndrome
| - 8600. Cystospy
- (UMLS (HL7) C1548842) =Health Care Activity =Consent Type;
|
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