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
A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
AM AMA AMB AMC AMD AME AMF AMG AMH AMI AML AMM AMN AMO AMP AMS AMT AMV AMY
selected terms: 578 page 6 of 6

501. AMPUTAT FOOT, BILAT-COMP
[ ] (UMLS (ICD9CM) C0273419) =Injury or Poisoning
540. AMSA/ARA-C
(UMLS (NCI) C0278525) =Therapeutic or Preventive Procedure
502. AMPUTAT LEG, BILAT-COMPL
[ ] (UMLS (ICD9CM) C0160678) =Injury or Poisoning
541. AMSA/ARA-C/BCNU/VP-16
(UMLS (NCI) C0338282) =Therapeutic or Preventive Procedure ;
503. AMPUTAT LEG, UNILAT NOS
[ ] (UMLS (ICD9CM) C0160675) =Injury or Poisoning
542. AMSA/ARA-C/DNR
(UMLS (NCI) C0279007) =Therapeutic or Preventive Procedure ;
504. AMPUTAT STUMP COMPL NEC
[ ] (UMLS (ICD9CM) C0161825) =Disease or Syndrome ;
543. AMSA/ARA-C/PRED/VCR
(UMLS (NCI) C0051766) =Therapeutic or Preventive Procedure ;
505. AMPUTAT STUMP COMPL NOS
[ ] (UMLS (ICD9CM) C0161821) =Injury or Poisoning ;
544. AMSA/ARA-C/VP-16
(UMLS (NCI) C0286421) =Therapeutic or Preventive Procedure ;
506. AMPUTAT THROUGH MALLEOLI
(UMLS (ICD9CM) C0701169) =Therapeutic or Preventive Procedure
545. AMSA/AZA/VP-16
(UMLS (NCI) C0083355) =Therapeutic or Preventive Procedure
507. amputation
[removal of a limb or other appendage or outgrowth of the body. ( CSP )] (UMLS (CSP) C0002688) =Therapeutic or Preventive Procedure
546. AMSA/CTX/HU
(UMLS (NCI) C0280058) =Therapeutic or Preventive Procedure
508. Amputation
(UMLS (HL7) C1546539) =Intellectual Product =Specimen Source Codes;
547. AMSA/CTX/VP-16
(UMLS (NCI) C0278621) =Therapeutic or Preventive Procedure
509. Amputation and disarticulation of finger
[ ] (UMLS (ICD9CM) C0177646) =Therapeutic or Preventive Procedure
548. AMSA/VP-16
(UMLS (NCI) C0278922) =Therapeutic or Preventive Procedure
510. Amputation and disarticulation of thumb
[ ] (UMLS (ICD9CM) C0701842) =Therapeutic or Preventive Procedure ;
549. AMSH
[Cytokine-mediated signal transduction in the JAK-STAT cascade requires the involvement of adaptor molecules. One such signal-transducing adaptor molecule contains an SH3 domain that is required for induction of MYC and cell growth. This protein binds to the SH3 domain of the signal-transducing adaptor molecule, and plays a critical role in cytokine-mediated signaling for MYC induction and cell cycle progression. (LocusLink) ( NCI )] (UMLS (NCI) C1101604) AMSH Protein;
Associated Molecule with the SH3 Domain of STAM =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
511. AMPUTATION ARM, BILAT
[ ] (UMLS (ICD9CM) C0160640) =Injury or Poisoning
550. Amsidyl
(UMLS (NCI) C0919345) =Organic Chemical; Pharmacologic Substance ;
512. AMPUTATION FINGER
[ ] (UMLS (ICD9CM) C0160631) =Injury or Poisoning
551. AMV
(UMLS (NCI) C0280591) =Therapeutic or Preventive Procedure
513. AMPUTATION FINGER-COMPL
[ ] (UMLS (ICD9CM) C0160632) =Injury or Poisoning
552. AMVP
(UMLS (NCI) C0279219) =Therapeutic or Preventive Procedure
514. AMPUTATION FOOT, BILAT
[ ] (UMLS (ICD9CM) C0160668) =Injury or Poisoning
553. AMYB
[A DNA-binding, transcriptional activator with a possible role in proliferation and/or differentiation of neurogenic, spermatogenic and B-lymphoid cells. A-Myb specifically recognizes the DNA sequence 5'-YAAC(G/T)G-3' and belongs to the Myb family. (from SWISS-PROT P10243, OMIM 159405, and NCI) ( NCI )] (UMLS (NCI) C0258050) =Amino Acid, Peptide, or Protein; Biologically Active Substance
515. AMPUTATION FOOT, UNILAT
(UMLS (ICD9CM) C1366330) Traumatic amputation of foot (complete) (partial), unilateral, without mention of complication =Injury or Poisoning
554. amygdala
[almond-shaped group of basal nuclei anterior to the inferior horn of the lateral ventricle of the brain, within the temporal lobe; part of the limbic system. ( CSP )] (UMLS (CSP) C0002708) =Body Part, Organ, or Organ Component
516. AMPUTATION LEG, BILAT
[ ] (UMLS (ICD9CM) C0160677) =Injury or Poisoning
555. Amygdalin
[A cyanogenic glucoside isolated from almonds and seeds of other plants of the family Rosaceae. Amygdalin is converted by plant emulsin (a combination of a glucosidase and a nitrilase) or hydrochloric acid into benzaldehyde, D-glucose, and hydrocyanic acid. (NCI04) ( NCI )] (UMLS (NCI) C0002707) =Carbohydrate; Pharmacologic Substance ;
517. Amputation Neuroma
(UMLS (NCI) C0392617) =Disease or Syndrome
556. amyl nitrite
[A vasodilator that is administered by inhalation. It is also used recreationally due to its supposed ability to induce euphoria and act as an aphrodisiac. ( MSH )] (UMLS (CSP) C0002711) =Organic Chemical; Pharmacologic Substance ;
518. AMPUTATION OF CERVIX
(UMLS (ICD9CM) C0195331) =Therapeutic or Preventive Procedure
557. amylase
[(AM-il-aze) An enzyme that helps the body digest starches. ( NCI )] (UMLS (CSP) C0002712) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Enzyme
519. Amputation of Foot
(UMLS (NCI) C0188605) =Therapeutic or Preventive Procedure
558. Amylase
[A measurement of the pancreatic enzyme amylase in a biological specimen. ( NCI )] (UMLS (NCI) C0201883) =Laboratory Procedure
520. Amputation of Leg Through Tibia and Fibula
(UMLS (NCI) C0002692) =Therapeutic or Preventive Procedure
559. amylase inhibitor
[ ] (UMLS (CSP) C0597832) =Pharmacologic Substance =enzyme inhibitor;
521. Amputation of lower limb
[ ] (UMLS (ICD9CM) C0337308) =Therapeutic or Preventive Procedure
560. amylin
[37-amino acid polypeptide occurring packaged with insulin in the beta cell secretory granules in normal pancreatic islets; also, a major component of islet amyloid in patients with noninsulin dependent diabetes mellitus. ( CSP )] (UMLS (CSP) C0063684) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Hormone =Interacinar Cell Pancreatic Polypeptide;
522. Amputation of penis
[ ] (UMLS (ICD9CM) C0194708) =Therapeutic or Preventive Procedure
561. amylo 1,4:1,6 transglucosidase deficiency
[ ] (UMLS (CSP) C0677581) =Disease or Syndrome
523. Amputation of toe
[ ] (UMLS (ICD9CM) C0188602) =Therapeutic or Preventive Procedure
562. amylo 1,6 glucosidase
[ ] (UMLS (CSP) C0051775) =Amino Acid, Peptide, or Protein; Enzyme
524. Amputation of upper limb
[ ] (UMLS (ICD9CM) C0186399) =Therapeutic or Preventive Procedure
563. amylo 1,6 glucosidase deficiency
[autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase; clinical course is similar to that of glycogen storage disease type I, but milder; massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age; levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. ( CSP )] (UMLS (CSP) C0017922) =Disease or Syndrome =glycogen storage disease;
525. Amputation stump complication
[ ] (UMLS (ICD9CM) C0302473) =Pathologic Function
564. Amyloid Beta (A4) Precursor Protein (Protease Nexin-II, Alzheimer Disease) Gene
[This gene is involved in transcriptional activation and mutations in the gene are correlated with Alzheimer disease. ( NCI )] (UMLS (NCI) C1364818) APP;
APP Gene;
=Gene or Genome
526. AMPUTATION STUMP REVIS
[ ] (UMLS (ICD9CM) C0185432) =Therapeutic or Preventive Procedure
565. Amyloid Beta Precursor Protein (Cytoplasmic Tail) Binding Protein 2
[Encoded by human APPBP2 Gene, ubiquitous 70 kD cytoplasmic Amyloid Beta Precursor Protein-Binding Protein 2 contains terminal globular structures, a coiled coil domain, PKC phosphorylation sites, and four imperfect C-terminal tandem repeats. In the Golgi apparatus, APPBP2 is associated with transport or processing of amyloid precursor protein (APP). Cell surface sorting of the signal-transducing APP depends on a cytoplasmic tyrosine-based basolateral sorting signal (BaSS) sequence to which APPBP2 specifically binds. Amyloid BaSS tyrosine mutation prevents APPBP2 binding and results in nonpolarized transport. Similar to the kinesin light chain, APPBP2 also interacts with microtubules and may have a role in vesicle sorting. APPBP2 is abundantly expressed in breast cancer. (from OMIM, and NCI) ( NCI )] (UMLS (NCI) C1332256) Amyloid Beta Precursor Protein-Binding Protein 2;
APPBP2;
PAT1 Protein;
Protein Interacting with APP Tail 1 =Amino Acid, Peptide, or Protein; Biologically Active Substance
527. AMPUTATION THROUGH FOOT
[ ] (UMLS (ICD9CM) C0812427) Transmetatarsal Amputation of Foot;
=Therapeutic or Preventive Procedure ;
566. Amyloid Beta Precursor Protein (Cytoplasmic Tail) Binding Protein 2 Gene
[This gene plays a role in the regulation of protein transport and microtubule dynamics. The gene has also been implicated in the pathogenesis of Alzheimer's disease. ( NCI )] (UMLS (NCI) C1332104) APPBP2;
APPBP2 Gene =Gene or Genome ;
528. Amputation through forearm
[ ] (UMLS (ICD9CM) C0186539) =Therapeutic or Preventive Procedure
567. Amyloid Beta-Peptide Pathway
[Alzheimer's disease is associated with dense aggregations of proteins in the brain called amyloid plaques that contain beta-amyloid fragments as a primary component. If the development of amyloid plaques is responsible for neurodegeneration in Alzheimer's disease, reduction of beta-amyloid formation may prevent the development and progression of disease symptoms. Beta-amyloid fragments are derived from proteolytic processing of amyloid precursor protein (APP) in neurons, and the subsequent release of fragments into the extracellular space. APP in the ER is cleaved at residue 17 by alpha-secretase protease activity encoded by ADAM-10 and TACE. Beta-secretase activity, recently identified as BACE, cleaves in the N-terminus of the beta-amyloid fragment. Gamma-secretase cuts APP within the transmembrane domain at amino acids 40 and 42, releasing the beta-amyloid fragment containing residues 1-40/42 as well as shorter products such as p3 (residues 17-40/42) that requires alpha-secretase cleavage. The gamma-secretase activity requires the transmembrane protein Presenilin-1 that is itself cleaved into an N-terminal and C-terminal fragment that both are required for gamma-secretase activity. Mutations in presenilin-1 have been genetically associated with familial forms of Alzheimer's disease, further supporting the role of APP processing the development of the disease. Inhibition of the beta- or gamma-secretases may provide a mechanism to treat this disease. Other mechanisms may include altering degradation of beta-amyloid, and the use of vaccines against beta-amyloid to remove aggregates. (BioCarta) ( NCI )] (UMLS (NCI) C1510880) Generation of amyloid b-peptide by PS1;
=Molecular Function ;
529. AMPUTATION THROUGH HAND
[ ] (UMLS (ICD9CM) C0187278) =Therapeutic or Preventive Procedure
568. amyloid disease
[any disease manifested by the pathogenic accumulation of amyloid in organs and tissues. ( CSP )] (UMLS (CSP) C0002726) =Disease or Syndrome
530. Amputation through humerus
(UMLS (ICD9CM) C0392807) =Therapeutic or Preventive Procedure ;
569. Amyloid Fibril Interaction
[Amyloid Fibril Interaction involves temporary non-covalent binding of a molecule through intermolecular physical forces of attraction with insoluble forms of a secretase-processed metal ion-binding type I cell surface glycoprotein (APP Family) required for endocytosis and BaSS sorting; important in developing synapses, for cell mobility, adhesion, and axonogenesis; and Notch signaling inhibitor, copper homeostasis regulator, transcription activator, and apoptosis enhancer. ( NCI )] (UMLS (NCI) C1510881) =Molecular Function ;
531. AMPUTATION THUMB
[ ] (UMLS (ICD9CM) C0433638) =Injury or Poisoning
570. amyloid precursor protein
[A precursor to the AMYLOID-BETA PROTEIN (beta/A4). Alterations in the expression of the amyloid beta-protein precursor (ABPP) gene, located on chromosome 21, plays a role in the development of the neuropathology common to both ALZHEIMER DISEASE and DOWN SYNDROME. ABPP is associated with the extensive extracellular matrix secreted by neuronal cells. Upon cleavage, this precursor produces three proteins of varying amino acid lengths: 695, 751, and 770. The beta/A4 (695 amino acids) or beta-amyloid protein is the principal component of the extracellular amyloid in senile plaques found in ALZHEIMER DISEASE; DOWN SYNDROME and, to a limited extent, in normal aging. ( MSH )] (UMLS (CSP) C0085151) =Amino Acid, Peptide, or Protein ;
532. AMPUTATION THUMB-COMPL
[ ] (UMLS (ICD9CM) C0160629) =Injury or Poisoning
571. Amyloid Precursor Protein Secretase
[Cathepsin B, encoded by the CTSB Gene, encodes a lysosomal cysteine proteinase composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor. It is also known as amyloid precursor protein secretase and is involved in the proteolytic processing of amyloid precursor protein (APP). Incomplete proteolytic processing of APP has been suggested to be a causative factor in Alzheimer disease, the most common cause of dementia. Overexpression of Cathepsin B has been associated with esophageal adenocarcinoma and other tumors. Tumors with overexpression of cathepsins have powerful potential for invasiveness in the early stage of gastric carcinoma. Gastric carcinoma cells that oversecrete cathepsins B have a high invasive and metastatic potential. At least five transcript variants encoding the same protein have been found for this gene. (From LocusLink, PMID 10931446 and NCI) ( NCI )] (UMLS (NCI) C0699919) =Amino Acid, Peptide, or Protein; Enzyme =caspase;
533. AMPUTATION TOE
[ ] (UMLS (ICD9CM) C0160662) =Injury or Poisoning
572. amyloid protein
[extracellular glycoprotein that accumulates in certain pathological conditions, e.g., the paired helical filaments of neuritic plaques in Alzheimer's disease and Down's syndrome; use this term for both the precursor and beta form. ( CSP )] (UMLS (CSP) C1456454) =Amino Acid, Peptide, or Protein; Biologically Active Substance =glycoprotein;
fibrous protein
534. AMPUTATION TOE-COMPLICAT
[ ] (UMLS (ICD9CM) C0433625) =Injury or Poisoning
573. Amyloid Resorption Induction
[Amyloid Resorption Induction involves initiation of activities of involved in the breakdown and assimilation of amyloid deposits. ( NCI )] (UMLS (NCI) C1510882) =Molecular Function ;
535. Amputee
(UMLS (HL7) C1546421) =Finding =Ambulatory Status;
574. Amyloidoma
[Amyloidoma - nodular localized form of amyloidosis with predominantly thoracic localization (pulmonary amyloidosis), considered as secondary protein structure diseases in which insoluble protein fibrils accumulate extracellularly. The form of primary amyloid in amyloidoma is characterized by abnormal deposition of light chain proteins composed of monoclonal immunoglobulin. Pulmonary amyloidomas are rare and are often found incidentally as solitary or multiple calcified nodules and masses on chest radiographs in asymptomatic elderly patients. Cavitation is rare, the prognosis is good. ( NCI )] (UMLS (NCI) C0544840) =Neoplastic Process
536. Amputee
[An entity, facility, or distinct part of a facility providing counseling, fitting, custom design, prescriptive, and training services related to congenital or postoperative absence of all or part of a limb or limbs. ( HL7V3.0 )] (UMLS (HL7) C1552524) =Manufactured Object; Health Care Related Organization =Clinic/Center;
575. AMYLOIDOSIS NEC
[ ] (UMLS (ICD9CM) C0348499) =Disease or Syndrome
537. Amputee clinic
(UMLS (HL7) C1552766) =Intellectual Product ;
=Outpatient facility;
576. amylopectinosis
[autosomal recessive metabolic disorder due to a deficiency in expression of branching enzyme (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches; clinical features are muscle hypotonia and cirrhosis; death from liver disease usually occurs before age 2. ( CSP )] (UMLS (CSP) C0017923) =Disease or Syndrome =glycogen storage disease;
538. Amsa P-D
(UMLS (NCI) C0591085) =Organic Chemical; Pharmacologic Substance
577. amylophosphorylase
[mobilizes glucose-1-phosphate from glycogen in muscle and other tissues do not use as a general term to cover other phosphorylases (see PHOSPHOTRANSFERASE). ( CSP )] (UMLS (CSP) C0917783) muscle phosphorylase;
phosphorylase;
polyphosphorylase;
=Amino Acid, Peptide, or Protein; Enzyme ;
=hexosyltransferase;
539. AMSA/5-AZA-dCyd
(UMLS (NCI) C0279490) =Therapeutic or Preventive Procedure
578. amyotonia congenita
[congenital atonic pseudoparalysis observed especially in infants and characterized by absence of muscular tone only in muscles innervated by the spinal nerves; also known as Oppenheim's disease or syndrome or congenital atonic pseudoparalysis. ( CSP )] (UMLS (CSP) C0002735) =Congenital Abnormality; Disease or Syndrome ;

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