- 7501. Ankylosis of upper arm joint
- [ ] (UMLS (ICD9CM) C0158120) =Acquired Abnormality; Disease or Syndrome
| - 7551. ANOMALIES OF FOOT NEC
- [ ] (UMLS (ICD9CM) C0868868) Anomalies of foot, congenital, NEC =Congenital Abnormality
|
- 7502. ankyrin
- [loosely associated membrane protein which links spectrin to integral membrane proteins such as "band 3." ( CSP )] (UMLS (CSP) C0051926) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
=cytoskeletal protein;
| - 7552. Anomalies of gallbladder, bile ducts, and liver
- [ ] (UMLS (ICD9CM) C0158681) =Congenital Abnormality ;
|
- 7503. Ankyrin Repeat Domain 30A
- [Encoded by human Breast Cancer Antigen NY-BR-1 Gene expressed in breast and testis, the 1341-amino acid 152 kD NY-BR-1 Protein contains an apparent DNA-binding bZIP motif and five tandem ankyrin repeats, implying a transcription factor involved in protein-protein interactions. (from Cancer Res 2001; 61:2055, SWISS-PROT, LocusLink, and NCI) ( NCI )] (UMLS (NCI) C1332617) Breast Cancer Antigen NY-BR-1;
NY-BR-1;
=Amino Acid, Peptide, or Protein; Biologically Active Substance | - 7553. Anomalies of great veins, congenital
- [ ] (UMLS (ICD9CM) C0158632) =Congenital Abnormality ;
|
- 7504. Ankyrin Repeat-Containing Protein KRIT1
- [Ankyrin Repeat-Containing Protein KRIT1, encoded by the CCM1 gene, interacts with ICAP-1 and may be involved in bidirectional signaling between integrin molecules and the cytoskeleton. KRIT1 may help determine endothelial cell shape and function in response to cell-cell and cell-matrix interactions by guiding cytoskeletal structure. Defects in the CCM1 gene are responsible for the development of cerebral cavernous malformations, a relatively rare disease causing vascular malformations that may involve any part of the central nervous system. KRIT1 may affect cell adhesion processes via integrin signaling in CCM1 pathogenesis. KRIT1 also interacts with RAP1A (a member of the Ras family of GTPases) and may be involved in the RAP1A signal transduction pathway in vasculogenesis or angiogenesis. KRIT1 contains 4 ankyrin repeats, 1 band 4.1-like domain, and 1 FERM domain. (From NCI) ( NCI )] (UMLS (NCI) C1366911) CAM;
CCM1;
Cerebral Cavernous Malformations 1;
Krev Interaction Trapped 1;
KRIT1 =Amino Acid, Peptide, or Protein; Biologically Active Substance | - 7554. ANOMALIES OF INNER EAR
- (UMLS (ICD9CM) C0685874) =Congenital Abnormality
|
- 7505. Ann Arbor Lymphoma Staging System
- [The Ann Arbor system classifies lymphoma into four stages based on anatomic lymph nodal group involvement. Disease confined to one nodal group or location defines stage I. Disease limited to one side of the diaphragm, (the muscle separating the chest from the abdomen), defines stage II. Stage III patients have disease on both sides of the diaphragm and stage IV patients once again have disseminated disease. Consideration of involvement of the liver, spleen, and bone marrow are also considered in this system. Finally, the stage is subdivided into categories of A and B depending on the presence of symptoms of itching, weight loss, fever, and night sweats. Those having symptoms receive the designation "B" and have a worse prognosis. ( NCI )] (UMLS (NCI) C0432516) =Classification
| - 7555. Anomalies of intestinal fixation, congenital
- [ ] (UMLS (ICD9CM) C0158679) =Congenital Abnormality ;
|
- 7506. Annamycin
- [A lipophilic, anthracycline antineoplastic antibiotic. Annamycin intercalates into DNA and interacts with topoisomerase II, thereby inhibiting DNA replication and repair and RNA and protein synthesis. This agent also circumvents multidrug-resistance (MDR) transporters, including p-glycoprotein. (NCI04) ( NCI )] (UMLS (NCI) C0214529) =Organic Chemical; Pharmacologic Substance ;
| - 7556. ANOMALIES OF LENS SHAPE
- [ ] (UMLS (ICD9CM) C0158553) =Congenital Abnormality ;
|
- 7507. Annamycin Liposomal
- [A liposome-encapsulated form of the antineoplastic antibiotic annamycin. Annamycin intercalates into DNA and interacts with topoisomerase II, thereby inhibiting DNA replication and repair and RNA and protein synthesis. This agent also circumvents multidrug-resistance (MDR) transporters, including p-glycoprotein. Less toxic than annamycin, liposomal annamycin also shows improved antitumor properties compared to its parent compound. (NCI04) ( NCI )] (UMLS (NCI) C0935796) =Organic Chemical; Pharmacologic Substance ;
| - 7557. Anomalies of other endocrine glands, congenital
- [ ] (UMLS (ICD9CM) C0432378) =Congenital Abnormality
|
- 7508. annealing of DNA
- [ ] (UMLS (CSP) C0920681) =Molecular Function ;
| - 7558. ANOMALIES OF OVARIES
- [ ] (UMLS (ICD9CM) C0158688) =Congenital Abnormality ;
|
- 7509. annealing of RNA
- [ ] (UMLS (CSP) C0920395) =Molecular Function ;
| - 7559. Anomalies of pancreas, congenital
- [ ] (UMLS (ICD9CM) C0158684) =Congenital Abnormality ;
|
- 7510. Annelida
- [phylum of metazoan invertebrates comprising the segmented worms, and including marine annelids (Polychaeta), freshwater annelids, earthworms (Oligochaeta), and Leeches. ( CSP )] (UMLS (CSP) C0003096) =Invertebrate ;
| - 7560. Anomalies of pulmonary artery, congenital
- (UMLS (ICD9CM) C0009681) =Congenital Abnormality ;
|
- 7511. annexin
- [family of proteins which bind phospholipids in the presence of calcium, believed to mediate intracellular calcium's role in membrane fusion and related events such as exocytosis; lipocortin and endonexin may also function extracellularly as inhibitors of phospholipase and blood coagulation. ( CSP )] (UMLS (CSP) C0065042) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
=calcium binding protein;
| - 7561. Anomalies of pulmonary valve, congenital
- (UMLS (ICD9CM) C0265830) =Congenital Abnormality ;
|
- 7512. Annexin A5 Gene
- [This gene is involved in anticoagulation processes and mediates lipid binding. ( NCI )] (UMLS (NCI) C1332095) ANXA5;
ANXA5 Gene =Gene or Genome ;
| - 7562. Anomalies of relationship of jaw to cranial base
- (UMLS (ICD9CM) C0003110) =Anatomical Abnormality ;
|
- 7513. Annexin A8
- [Annexin VIII belongs to the family of Ca (2+) dependent phospholipid binding proteins (annexins), and has a high 56% identity to annexin V (vascular anticoagulant-alpha). It was initially isolated as 2.2 kb vascular anticoagulant-beta transcript from human placenta, a Ca (2+) dependent phospholipid binding protein that inhibits coagulation and phospholipase A2 activity. However, the fact that annexin VIII is neither an extracellular protein nor associated with the cell surface suggests that it may not play a role in blood coagulation in vivo and its physiological role remains unknown. (LocusLink) ( NCI )] (UMLS (NCI) C0162710) =Amino Acid, Peptide, or Protein; Biologically Active Substance
| - 7563. ANOMALIES OF SCLERA
- (UMLS (ICD9CM) C0344538) =Congenital Abnormality ;
|
- 7514. Annexin A8 Gene
- [This gene plays a role in lipid binding regulation and the overexpression of the gene has been isolated in acute myelocytic leukemia. ( NCI )] (UMLS (NCI) C1332096) ANXA8;
ANXA8 Gene =Gene or Genome ;
| - 7564. Anomalies of spine, congenital
- [ ] (UMLS (ICD9CM) C0158775) =Congenital Abnormality ;
|
- 7515. Annona muricata
- [A common name for the tropical tree Annona muricata whose tissues contain annonaceous acetogenins, compounds with antineoplastic activity. Annonaceous acetogenins, derivatives of long-chain fatty acids, exhibit their anti-tumor properties by depleting cellular stores of adenosine 5'-triphosphate (ATP), a primary source of energy in cells. These agents also inhibit ATP-driven drug resistance mechanisms. Possessing a broad range of therapeutic activities, graviola has been used in different cultures for its pesticidal, antifungal,, antispasmodic, anticonvulsant, vasodilator, smooth-muscle relaxant, and hypotensive properties. (NCI04) ( NCI )] (UMLS (NCI) C1000635) Brazilian Cherimoya;
Brazilian Paw Paw;
Graviola;
Guanabana;
Prickly Custard Apple;
Soursop =Plant | - 7565. ANOMALIES OF SPLEEN
- (UMLS (ICD9CM) C0700587) =Congenital Abnormality ;
|
- 7516. Annotated
- (UMLS (HL7) C1552657) =Idea or Concept =Type;
◊ (UMLS (HL7) C1552720) Idea or Concept ANY; Annotated Concept Descriptor; Annotated Physical Quantity | - 7566. ANOMALIES OF TOES NEC
- (UMLS (ICD9CM) C0432018) =Congenital Abnormality ;
|
- 7517. Annotated Concept Descriptor
- (UMLS (HL7) C1552721) =Idea or Concept =Annotated;
| - 7567. Anomalies of tooth position of fully erupted teeth
- [ ] (UMLS (ICD9CM) C1456201) =Anatomical Abnormality
|
- 7518. Annotated Physical Quantity
- (UMLS (HL7) C1552722) =Idea or Concept =Annotated;
| - 7568. ANOMALIES OF URACHUS
- (UMLS (ICD9CM) C0431741) =Congenital Abnormality ;
|
- 7519. Annotations
- (UMLS (HL7) C1547713) =Idea or Concept =HL7 Vocabulary Version 2.5;
=Pace spike;
SAS marker;
Sense marker;
Beat marker;
etc.;
| - 7569. Anomalous atrioventricular excitation
- [ ] (UMLS (ICD9CM) C0392470) =Disease or Syndrome
|
- 7520. AnnotationType
- (UMLS (HL7) C1698585) =Intellectual Product ;
=ObservationType;
=ECGAnnotationType | - 7570. ANOMALY DENTAL ARCH NEC
- [ ] (UMLS (ICD9CM) C1456189) Other anomalies of dental arch relationship;
=Finding |
- 7521. AnnotationValue
- (UMLS (HL7) C1698253) =Qualitative Concept =ObservationValue;
=ECGAnnotationValue;
| - 7571. ANOMALY OF SPINE NEC
- (UMLS (ICD9CM) C0432138) =Congenital Abnormality ;
|
- 7522. Annual
- [Occurring or done each year. ( NCI )] (UMLS (NCI) C0332181) =Temporal Concept
| - 7572. Anomaly of tongue, congenital, unspecified
- [ ] (UMLS (ICD9CM) C0158662) =Congenital Abnormality ;
|
- 7523. Annual Screening
- (UMLS (NCI) C1134631) =Diagnostic Procedure
| - 7573. anomer
- [alpha or beta isomers of cyclic carbohydrates produced when a new point of symmetry arises after rearrangement of atoms at the aldehyde or ketone position. ( CSP )] (UMLS (CSP) C0596105) =Chemical Viewed Structurally ;
=isomer;
|
- 7524. Annular
- [Doughnut-shaped object or surface generated by rotating a circle around an axis that does not intersect the circle; any object that resembles a ring. ( NCI )] (UMLS (NCI) C0521164) =Spatial Concept
| - 7574. anomia
- [A language dysfunction characterized by the inability to name people and objects that are correctly perceived. The individual is able to describe the object in question, but cannot provide the name. This condition is associated with lesions of the dominant hemisphere involving the language areas, in particular the TEMPORAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, p484) ( MSH )] (UMLS (CSP) C0003113) =Mental or Behavioral Dysfunction ;
|
- 7525. Annulled
- [Marriage contract has been declared null and to not have existed ( HL7V3.0 )] (UMLS (HL7) C1549109) =Finding =marital status;
MaritalStatus | - 7575. Anonymous identifier
- (UMLS (HL7) C1549679) =Idea or Concept =Identifier type;
|
- 7526. ANNULOPLASTY
- [ ] (UMLS (ICD9CM) C0190165) =Therapeutic or Preventive Procedure
| - 7576. Anopheles
- [genus of mosquitoes in the family Culicidae that are known vectors of malaria. ( CSP )] (UMLS (CSP) C0003117) =Invertebrate ;
|
- 7527. annulus of the aqueduct
- [gray matter surrounding the narrow channel through the mesencephalon which connects the third and fourth ventricles of the brain. ( CSP )] (UMLS (CSP) C0228398) =Body Part, Organ, or Organ Component =tegmentum;
| - 7577. Anophthalmos
- [Congenital absence of the eye or eyes. ( MSH )] (UMLS (ICD9CM) C0003119) =Congenital Abnormality ;
|
- 7528. Anocutaneous Line
- [The line between the simple columnar epithelium of the rectum and the stratified epithelium of the anal canal. ( NCI )] (UMLS (NCI) C0922973) Pectinate Line. =Body Space or Junction
| - 7578. Anoplura
- [An order of insects comprising the sucking lice, which are blood-sucking ectoparasites of mammals. Recognized families include: Echinphthiriidae, Haematopinidae, and Pediculidae. The latter contains the medically important genera affecting humans: PEDICULUS and PHTHIRUS. ( MSH )] (UMLS (CSP) C0003121) =Invertebrate ;
|
- 7529. anode
- [ ] (UMLS (CSP) C0003103) =Manufactured Object ;
| - 7579. anorectal disorder
- [disturbance of structure, function, or both of the anus and/or rectum. ( CSP )] (UMLS (CSP) C0687707) =Disease or Syndrome ;
=Gastrointestinal Diseases;
=Afforingsinkontinens |
- 7530. ANODONTIA
- [Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed) ( MSH )] (UMLS (ICD9CM) C0399352) =Congenital Abnormality =congenital dentition disorder;
| - 7580. anorectal fistula
- [ ] (UMLS (CSP) C0149889) =Pathologic Function
|
- 7531. Anogenital Human Papilloma Virus Infection
- (UMLS (NCI) C0554632) =Disease or Syndrome
| - 7581. Anorectal myectomy
- [ ] (UMLS (ICD9CM) C0193056) =Therapeutic or Preventive Procedure
|
- 7532. Anogenital Papillomaviral Intraepithelial Neoplasia
- (UMLS (NCI) C0343652) =Neoplastic Process
| - 7582. anorexia
- [clinical manifestation consisting of a physiopathological lack or loss of appetite accompanied by an aversion to food and the inability to eat. ( CSP )] (UMLS (CSP) C0003123) =Sign or Symptom ;
|
- 7533. anoikis
- [Anoikis (detachment induced cell death or suspension induced apoptosis) is the name given to a special form of cell death by apoptosis. It was observed initially after disruption of the interactions between normal epithelial cells and extracellular matrix. In an intact organism anoikis ensures that cells are unable to survive in an inappropriate location. Anoikis thus is apoptosis caused by cell isolation or apoptosis of cells in suspension or, generally speaking, apoptosis caused by loss of adherence to substrate. (from Cytokines Online Pathfinder Encyclopaedia) ( NCI )] (UMLS (CSP) C0872097) Detachment-Induced Cell Death;
Suspension-Induced Apoptosis =Cell Function ;
| - 7583. anorexia nervosa
- [syndrome in which the primary features include excessive fear of becoming overweight, body image disturbance, significant weight loss, refusal to maintain minimal normal weight, and amenorrhea; disorder occurs most frequently in adolescent females. ( CSP )] (UMLS (CSP) C0003125) =Mental or Behavioral Dysfunction ;
|
- 7534. ANOM ANTER CHAMBER-EYE
- (UMLS (ICD9CM) C0701146) =Congenital Abnormality
| - 7584. Anorexia nervosa/bulimia
- (UMLS (ICPC) C0497397) (Anorexia nervosa/bulimia; URDURITASUN ANORESIA BULIMINAGAZ/GABE; Anorexia nervosa/bulimi; Anorexia nervosa/boulimie; ANOREXIA NERVOSA/BULIMIA; Anorexie nerveuse/boulimie; Anorexia nervosa/Bulimie; anoreksia nervoza; anorexia nervosa/bulimia; Anoressia nervosa/bulimia; SPISEVEGR/ANOREXIA NERVOSA/BULIMI; Anorexia nervosa com/sem bulimia; Anorexia nerviosa; ANOREXIA NERVOSA/BULIMI) =Disease or Syndrome =ENDOCRINE, METABOLIC AND NUTRITIONAL; Symptoms and Complaints Component
|
- 7535. ANOM ANTER SEG NEC-EYE
- [ ] (UMLS (ICD9CM) C0029552) =Congenital Abnormality ;
| - 7585. ANOSCOPY
- (UMLS (ICD9CM) C0193158) =Diagnostic Procedure
|
- 7536. ANOM CORNEAL SIZE/SHAPE
- (UMLS (ICD9CM) C0344528) =Congenital Abnormality ;
| - 7586. anosmia
- [absence of the sense of smell. ( CSP )] (UMLS (CSP) C0003126) =Sign or Symptom ;
|
- 7537. ANOM DIGESTIVE SYST NEC
- [ ] (UMLS (ICD9CM) C0478039) =Congenital Abnormality
| - 7587. Anosognostic Epilepsy
- (UMLS (NCI) C1332300) =Disease or Syndrome ;
|
- 7538. ANOM EYELID/LACR/ORB NEC
- [ ] (UMLS (ICD9CM) C0158579) =Disease or Syndrome ;
| - 7588. ANOVA
- [Expressed in brain by human NOVA2 Gene, RNA-binding NOVA2 protein is recognized by the paraneoplastic syndrome antibody anti-Ri. NOVA1 and NOVA2 bind to similar RNA ligands with high affinity and may regulate RNA splicing. The NOVA2 KH3 domain interacts with single-stranded RNA; KH3 bound to stem loop RNA resembles a vise, with UCAC held between an invariant Gly-X-X-Gly motif and a variable loop. Tetranucleotide recognition is supported by an aliphatic alpha-helix/beta-sheet RNA-binding platform that mimics UG by making Watson-Crick-like hydrogen bonds with CA. (NCI) ( NCI )] (UMLS (NCI) C1367971) Neuro-Oncological Ventral Antigen 2;
Neuro-Oncological Ventral Antigen 3;
NOVA2;
NOVA3 =Amino Acid, Peptide, or Protein; Biologically Active Substance |
- 7539. ANOM INTERARCH DISTANCE
- [ ] (UMLS (ICD9CM) C1456186) Anomalies of interarch distance;
=Disease or Syndrome | - 7589. Anovulation
- [Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy. ( MSH )] (UMLS (NCI) C0003128) =Disease or Syndrome ;
|
- 7540. ANOM IRIS & CIL BODY NEC
- [ ] (UMLS (ICD9CM) C0158560) =Disease or Syndrome ;
| - 7590. anoxia
- [Absence or reduction of oxygen in body tissue. (PSY94) ( NCI )] (UMLS (CSP) C0003130) =Pathologic Function ;
|
- 7541. ANOMAL SKULL/FACE BONES
- [ ] (UMLS (ICD9CM) C0495615) =Congenital Abnormality
| - 7591. anoxia neonatorum
- [ ] (UMLS (CSP) C0349478) =Disease or Syndrome
|
- 7542. ANOMALIES EAR OSSICLES
- [ ] (UMLS (ICD9CM) C0158587) =Congenital Abnormality ;
| - 7592. ANOXIC BRAIN DAMAGE
- (UMLS (ICD9CM) C0003132) =Pathologic Function ;
|
- 7543. Anomalies of abdominal wall, congenital
- (UMLS (ICD9CM) C0009680) =Congenital Abnormality ;
| - 7593. ANPB
- [Expressed in heart and vasculature by human NPR2 Gene (Guanylyl Cyclase Family), type I integral membrane protein Natriuretic Peptide Receptor B is the primary receptor for C-type natriuretic peptides that cause natriuresis, sodium excretion in the urine. NPR2 contains an extracellular ligand-binding domain, a membrane-spanning region, and an intracellular protein kinase homology domain, oligomerizing helical hinge region, and a C-terminal guanylyl cyclase catalytic domain activated upon receptor ligand binding. NPR2 seems to be more effectively stimulated by BNP than by ANP. NPR1 and NPR2 are ANP receptors with guanylate cyclase activity; NPR3 is probably responsible for ANP clearance from the circulation without a role in signal transduction. (NCI) ( NCI )] (UMLS (NCI) C0530295) =Amino Acid, Peptide, or Protein; Enzyme; Receptor
|
- 7544. ANOMALIES OF AORTIC ARCH
- [ ] (UMLS (ICD9CM) C0158629) =Congenital Abnormality ;
| - 7594. ANS
- [those neurons which regulate the contraction of smooth and cardiac muscle and the secretion of glands, by way of the general visceral efferent component of cranial and spinal nerves; contains two divisions, parasympathetic and sympathetic which provide double innervation to most organs by way of a two-neuron chain, the first neuron has its cell of origin in the brain or spinal cord and the second in an autonomic ganglion. ( CSP )] (UMLS (CSP) C0004388) =Body System ;
|
- 7545. Anomalies of cerebrovascular system, congenital
- [ ] (UMLS (ICD9CM) C0158638) =Congenital Abnormality ;
| - 7595. Ansaid
- (UMLS (NCI) C0700848) =Organic Chemical; Pharmacologic Substance ;
|
- 7546. Anomalies of cervix, vagina, and external female genitalia, congenital
- [ ] (UMLS (ICD9CM) C0158694) =Congenital Abnormality ;
| - 7596. Ansamycin Antibiotics
- [A group of anticancer drugs that belongs to the family of drugs called antineoplastic antibiotics. ( NCI )] (UMLS (NCI) C0051936) =Organic Chemical; Antibiotic ;
|
- 7547. Anomalies of dental arch relationship
- [ ] (UMLS (ICD9CM) C0155939) =Anatomical Abnormality ;
| - 7597. ANSI ASC X12 Health Care Provider Taxonomy, Level 1 - Type
- (UMLS (HL7) C1547441) =Intellectual Product =Health care provider type code;
|
- 7548. ANOMALIES OF DIAPHRAGM
- [ ] (UMLS (ICD9CM) C0158782) =Congenital Abnormality ;
| - 7598. ANSI ASC X12 Health Care Provider Taxonomy, Level 2 - Classification
- (UMLS (HL7) C1547442) =Intellectual Product =Health care provider classification;
|
- 7549. ANOMALIES OF DIVERGENCE
- [ ] (UMLS (ICD9CM) C0155347) =Sign or Symptom
| - 7599. ANSI ASC X12 Health Care Provider Taxonomy, Level 3 - specialization
- (UMLS (HL7) C1547443) =Idea or Concept =Health care provider area of specialization;
|
- 7550. Anomalies of fallopian tubes and broad ligaments, congenital
- [ ] (UMLS (ICD9CM) C0158689) =Congenital Abnormality ;
| - 7600. answering service
- [An automated answering machine used for less urgent cases and if the main purpose of contact is to leave a message or access an automated announcement. ( HL7V3.0 )] (UMLS (HL7) C1550703) =Idea or Concept =TelecommunicationAddressUse;
|
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