- 2101. Acute Myelogenous Leukemia 1 Translocation 1 Protein MTG8A
- [Encoded by human CBFA2T1 Gene, conserved 604-aa 67.6-kD ETO Protein is a putative MYND zinc finger transcription factor expressed as multiple isoforms in brain, heart, lung, pituitary, skeletal muscle, pancreas, placenta, testis, and ovary. MTG8B and MTG8C variants have distinct N-termini. One frameshifted MTG8 variant lacks C-terminal zinc fingers, a P/S/T-rich domain, and a coiled-coil structure. In AML-M2, t(8;21)(q22;q22) in stem cells produces a fused chimeric RUNX1-CBFA2T1 protein. Associated with NCOR/HDAC, this protein may repress transcription and differentiation in hematopoietic precursors. p14(ARF) may be a target of AML1-ETO. (from LocusLink, Swiss-Prot, OMIM, and NCI) ( NCI )] (UMLS (NCI) C0218234) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
| - 2151. Acute myocardial infarction, true posterior wall infarction, initial episode of care
- [ ] (UMLS (ICD9CM) C0155653) =Disease or Syndrome
|
- 2102. Acute Myeloid Leukaemias and Myelodysplastic Syndromes, Therapy-Related
- (UMLS (NCI) C1292776) Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome;
Therapy-Related AML and MDS =Neoplastic Process | - 2152. Acute myocardial infarction, true posterior wall infarction, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155654) =Disease or Syndrome
|
- 2103. Acute Myeloid Leukemia not Otherwise Categorized
- [This category of acute myeloid leukemias is morphology based and reflects the morphologic subtypes present in the French-American-British (FAB) classification scheme. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C1332151) =Neoplastic Process ;
| - 2153. Acute myocardial infarction, unspecified site, initial episode of care
- [ ] (UMLS (ICD9CM) C0155664) =Disease or Syndrome ;
|
- 2104. Acute Myeloid Leukemia with 11q23 (MLL) Abnormalities
- [An acute myeloid leukemia (AML) usually associated with monocytic features. Patients may present with disseminated intravascular coagulation. This AML has an intermediate survival. (WHO, 2001) ( NCI )] (UMLS (NCI) C1292775) Acute Myeloid Leukemia with 11q23 Abnormalities;
Acute Myeloid Leukemia, MLL =Neoplastic Process | - 2154. Acute myocardial infarction, unspecified site, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155665) =Disease or Syndrome ;
|
- 2105. Acute Myeloid Leukemia with Abnormal Marrow Eosinophils
- [An acute myeloid leukemia (AML) with inv(16)(p13q22) or t(16;16)(p13;q22);(CBF-beat/MYH11). This AML shows monocytic and granulocytic differentiation and the presence of a characteristically abnormal eosinophil component in the bone marrow. This type of AML has a favorable prognosis. (WHO, 2001) ( NCI )] (UMLS (NCI) C0522630) =Neoplastic Process
| - 2155. Acute myocarditis
- [ ] (UMLS (ICD9CM) C0155686) =Disease or Syndrome
|
- 2106. Acute Myeloid Leukemia with inv(16)(p13;q22)
- (UMLS (NCI) C1332154) Acute Myeloid Leukemia with inv(16)(p13;q22)(CBFb/MYH11);
"Acute Myeloid Leukemia, inv(16)(p13;q22)" =Neoplastic Process ;
| - 2156. ACUTE MYOCARDITIS NEC
- [ ] (UMLS (ICD9CM) C0155692) =Disease or Syndrome
|
- 2107. Acute Myeloid Leukemia with Multilineage Dysplasia
- [An acute myeloid leukemia (AML) with at least 20% blasts in the marrow or blood, and dysplasia in 2 or more myeloid cell lines. Dysplasia must be present in at least 50% of the cells of at least 2 cell lines. Patients with this type of AML often present with severe cytopenia. The presence of multilineage dysplasia has an adverse effect on the probability of achieving complete remission. (WHO, 2001) ( NCI )] (UMLS (NCI) C1292773) =Neoplastic Process
| - 2157. ACUTE MYRINGITIS NEC
- [ ] (UMLS (ICD9CM) C0155462) =Disease or Syndrome
|
- 2108. Acute Myeloid Leukemia with Multilineage Dysplasia following Myelodysplastic Syndrome
- [A subtype of acute myeloid leukemia with multilineage dysplasia. This subtype includes the vast majority of refractory anemia with excess blasts in transformation cases. This latter term used to be part of the French-American-British classification scheme of myelodysplastic syndromes and has been eliminated from the WHO classification. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C1332153) AML/MDS;
=Neoplastic Process ;
| - 2158. ACUTE MYRINGITIS NOS
- [ ] (UMLS (ICD9CM) C0155460) =Disease or Syndrome
|
- 2109. Acute Myeloid Leukemia with Recurrent Genetic Abnormalities
- [A group of acute myeloid leukemias (AMLs) characterized by recurrent genetic abnormalities, mainly balanced translocations. This group of AMLs often has a high rate of complete remission, and favorable prognosis. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C1275661) =Neoplastic Process
| - 2159. Acute myringitis without mention of otitis media
- [ ] (UMLS (ICD9CM) C0155459) =Disease or Syndrome
|
- 2110. Acute Myeloid Leukemia with t(16;16)(p13;q22)
- (UMLS (NCI) C1332155) Acute Myeloid Leukemia, t(16;16)(p13;q22);
=Neoplastic Process ;
| - 2160. Acute Necrotizing Encephalitis
- (UMLS (NCI) C0338418) =Disease or Syndrome
|
- 2111. Acute Myeloid Leukemia with t(8;21)(q22;q22)
- [An acute myeloid leukemia (AML) showing maturation in the neutrophil lineage. The bone marrow and the peripheral blood show large myeloblasts with abundant basophilic cytoplasm, often containing azurophilic granules. This type of AML is associated with good response to chemotherapy and high complete remission rate. (WHO, 2001) ( NCI )] (UMLS (NCI) C1292774) Acute Myeloid Leukemia with t(8;21)(q22;q22)(AML1(CBFa)/ETO);
=Neoplastic Process | - 2161. Acute nonparalytic poliomyelitis
- [ ] (UMLS (ICD9CM) C0152998) =Disease or Syndrome
|
- 2112. Acute Myeloid Leukemia-1 Protein
- [Part of the heterodimeric transcription factor Core-Binding Factor. The CBFalpha subunit binds directly to the enhancer core DNA sequence on target genes, whereas the beta subunit does not bind the DNA directly but increases the affinity and stabilizes the binding of the alpha subunit to the DNA. Three homologous genes can encode for the CBFalpha subunit. Disruption of CBFA2 is associated with many leukemias, including AML, ALL, and CML. ( NCI )] (UMLS (NCI) C0215508) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
| - 2162. Acute nonparalytic poliomyelitis, poliovirus type I
- [ ] (UMLS (ICD9CM) C1112685) NONPARALYT POLIO-TYPE 1 =Disease or Syndrome ;
|
- 2113. Acute Myeloid Leukemia-1/Eight-Twenty-One Protein
- [In acute myeloid leukemia, the frequent t(8;21)(q22;q22) translocation produces a chimeric AML1/ETO gene. Association of the AML1/ETO product with the NCOR/HDAC complex blocks hematopoietic differentiation. The interaction requires ETO coiled-coil regions and is responsible for abnormal recruitment of NCOR, transcriptional repression, and impaired differentiation of primary hematopoietic precursors. AML1/ETO transcripts are present in a fraction of stem cells, monocytes, marrow B-cells, and in colony-forming cells of erythroid, granulocyte-macrophage, and/or megakaryocyte lineages, but not in T-cells. (from OMIM 133435 and NCI) ( NCI )] (UMLS (NCI) C1332085) AML-1/ETO =Amino Acid, Peptide, or Protein ;
| - 2163. Acute nonparalytic poliomyelitis, poliovirus type II
- [ ] (UMLS (ICD9CM) C1112686) NONPARALYT POLIO-TYPE 2 =Disease or Syndrome ;
|
- 2114. Acute Myelomonocytic Leukemia in Remission
- (UMLS (NCI) C0836973) =Neoplastic Process
| - 2164. Acute nonparalytic poliomyelitis, poliovirus type III
- [ ] (UMLS (ICD9CM) C1112687) NONPARALYT POLIO-TYPE 3 =Disease or Syndrome ;
|
- 2115. Acute Myelomonocytic Leukemia with Abnormal Eosinophils
- (UMLS (NCI) C1332156) AMML Eo;
FAB M4Eo =Neoplastic Process ;
| - 2165. Acute Obstructive Laryngitis
- [A condition characterized by resonant barking cough, hoarseness and persistant stridor and caused by allergy, foreign body, infection, or neoplasm. It occurs chiefly in infants and children. ( MSH )] (UMLS (NCI) C0010380) =Disease or Syndrome =laryngitis;
|
- 2116. Acute myocardial infarction
- (UMLS (ICPC) C0155626) (Acute myocardial infarction; MIOKARDIOKO INFARKTU ZORROTZA; Akut hjerteinfakt; Acuut myocard infarct; AKILLINEN SYDANINFARKTI; Infarctus myocardique aigu; akuter Myokardinfarkt; (108); acut myocardialis infarctus; Infarto miocardico acuto; AKUTT HJERTEINFARKT - i21 - i22 - i23 - i24; Enfarte agudo do miocardio; Infarto agudo de miocardio; AKUT HJARTINFARKT) =Disease or Syndrome =CIRCULATORY; Diagnosis/Diseases Component
| - 2166. ACUTE OTITIS EXTERNA NEC
- [ ] (UMLS (ICD9CM) C0155399) =Disease or Syndrome
|
- 2117. Acute myocardial infarction, of anterolateral wall
- [ ] (UMLS (ICD9CM) C0155627) =Disease or Syndrome
| - 2167. Acute otitis media/myringitis
- (UMLS (ICPC) C0497226) (Acute otitis media/myringitis; ERDI MAILAKO OTITIS ZORROTZA/MIRINGITISA; Akut mellemorebetaendelse/myringit; Otitis media acute/myringitis; MYRINGIITTI/ AKILLINEN VALIKORVATULEHDUS; Otite moyenne aigue/myringite; akute Otitis media/Trommelfellentz; daleket ozen xarifa; otitis media acuta/myringitis; Otite media/miringite acuta; AKUTT MELLOMOREBETENN/MYRINGITT; Otite media aguda/miringite; Otitis media aguda/miringitis; AKUT OTITIS MEDIA/ MELLANORONINFLAMMATION/TRUMHINNEINFLAMMATION) =Disease or Syndrome =auris; Diagnosis/Diseases Component
|
- 2118. Acute myocardial infarction, of anterolateral wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155628) =Disease or Syndrome
| - 2168. acute pain
- [Pain that comes on quickly, can be severe, but lasts a relatively short time. ( NCI )] (UMLS (NCI) C0184567) =Sign or Symptom ;
|
- 2119. Acute myocardial infarction, of anterolateral wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155629) =Disease or Syndrome
| - 2169. ACUTE PAIN DUE TO TRAUMA
- [ ] (UMLS (ICD9CM) C1719389) =Disease or Syndrome ;
|
- 2120. Acute myocardial infarction, of anterolateral wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155630) =Disease or Syndrome
| - 2170. ACUTE PAIN NEC
- [ ] (UMLS (ICD9CM) C1719723) Other acute pain =Disease or Syndrome
|
- 2121. Acute myocardial infarction, of inferolateral wall
- [ ] (UMLS (ICD9CM) C0340308) =Disease or Syndrome
| - 2171. ACUTE PANCREATITIS
- (UMLS (ICD9CM) C0001339) =Disease or Syndrome ;
|
- 2122. Acute myocardial infarction, of inferolateral wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155636) =Disease or Syndrome
| - 2172. Acute paralytic poliomyelitis specified as bulbar
- [A form of paralytic poliomyelitis affecting neurons of the MEDULLA OBLONGATA of the brain stem. Clinical features include impaired respiration, HYPERTENSION, alterations of vasomotor control, and dysphagia. Weakness and atrophy of the limbs and trunk due to spinal cord involvement is usually associated. (From Adams et al., Principles of Neurology, 6th ed, p765) ( MSH )] (UMLS (ICD9CM) C0032372) =Disease or Syndrome =Acute Poliomyelitis;
|
- 2123. Acute myocardial infarction, of inferolateral wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155637) =Disease or Syndrome
| - 2173. ACUTE PARAMETRITIS
- [ ] (UMLS (ICD9CM) C0156329) =Disease or Syndrome ;
|
- 2124. Acute myocardial infarction, of inferolateral wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155638) =Disease or Syndrome
| - 2174. ACUTE PARANOID REACTION
- (UMLS (ICD9CM) C0152125) =Mental or Behavioral Dysfunction
|
- 2125. Acute myocardial infarction, of inferoposterior wall
- [ ] (UMLS (ICD9CM) C0340304) =Disease or Syndrome
| - 2175. ACUTE PEPTIC ULCER NOS
- [ ] (UMLS (ICD9CM) C0267298) =Disease or Syndrome ;
|
- 2126. Acute myocardial infarction, of inferoposterior wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155640) =Disease or Syndrome
| - 2176. Acute peptic ulcer of unspecified site with hemorrhage and perforation
- [ ] (UMLS (ICD9CM) C0267294) =Disease or Syndrome ;
|
- 2127. Acute myocardial infarction, of inferoposterior wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155641) =Disease or Syndrome
| - 2177. Acute peptic ulcer of unspecified site with perforation
- [ ] (UMLS (ICD9CM) C0267291) =Disease or Syndrome ;
|
- 2128. Acute myocardial infarction, of inferoposterior wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155642) =Disease or Syndrome
| - 2178. Acute peptic ulcer of unspecified site without mention of hemorrhage and perforation
- [ ] (UMLS (ICD9CM) C0392499) =Disease or Syndrome
|
- 2129. Acute myocardial infarction, of other anterior wall
- [ ] (UMLS (ICD9CM) C0155631) =Disease or Syndrome
| - 2179. Acute pericarditis
- [ ] (UMLS (ICD9CM) C0155679) =Disease or Syndrome ;
|
- 2130. Acute myocardial infarction, of other anterior wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155632) =Disease or Syndrome
| - 2180. ACUTE PERICARDITIS NEC
- [ ] (UMLS (ICD9CM) C0348597) =Disease or Syndrome
|
- 2131. Acute myocardial infarction, of other anterior wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155633) =Disease or Syndrome
| - 2181. ACUTE PERIODONTITIS
- (UMLS (ICD9CM) C0001342) =Disease or Syndrome ;
|
- 2132. Acute myocardial infarction, of other anterior wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155634) =Disease or Syndrome
| - 2182. ACUTE PETROSITIS
- [ ] (UMLS (ICD9CM) C0155449) =Disease or Syndrome ;
|
- 2133. Acute myocardial infarction, of other inferior wall
- [ ] (UMLS (ICD9CM) C0155643) =Disease or Syndrome
| - 2183. ACUTE PHARYNGITIS
- (UMLS (ICD9CM) C0001344) =Disease or Syndrome
|
- 2134. Acute myocardial infarction, of other inferior wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155644) =Disease or Syndrome
| - 2184. acute phase protein
- [blood proteins that are produced in response to acute illness; including fibrinogen, ceruloplasmin, certain enzyme inhibitors and C reactive protein. ( CSP )] (UMLS (CSP) C0001347) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
|
- 2135. Acute myocardial infarction, of other inferior wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155645) =Disease or Syndrome
| - 2185. Acute Pneumonia
- (UMLS (NCI) C0740766) =Disease or Syndrome ;
|
- 2136. Acute myocardial infarction, of other inferior wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155646) =Disease or Syndrome
| - 2186. Acute Poliomyelitis
- [acute infectious disease of humans, particularly children, caused by any of three serotypes of human poliovirus; infection is usually limited to the gastrointestinal tract and nasopharynx, and is often asymptomatic; the central nervous system, primarily the spinal cord, may be affected, leading to rapidly progressive paralysis, coarse fasciculation and hyporeflexia; motor neurons are primarily affected and encephalitis may also occur; replicates in the nervous system, and may cause significant neuronal loss, most notably in the spinal cord. ( CSP )] (UMLS (NCI) C0032371) =Disease or Syndrome =Enterovirus Infections;
myelitis;
Infection, Viral;
degenerative motor system disease;
nervous system infection;
=Acute paralytic poliomyelitis specified as bulbar;
postpolio syndrome;
|
- 2137. Acute myocardial infarction, of other lateral wall
- [ ] (UMLS (ICD9CM) C0155647) =Disease or Syndrome
| - 2187. Acute poliomyelitis with other paralysis
- [ ] (UMLS (ICD9CM) C0152993) =Disease or Syndrome
|
- 2138. Acute myocardial infarction, of other lateral wall, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155648) =Disease or Syndrome
| - 2188. Acute poliomyelitis with other paralysis, poliovirus type I
- [ ] (UMLS (ICD9CM) C0152995) =Disease or Syndrome
|
- 2139. Acute myocardial infarction, of other lateral wall, initial episode of care
- [ ] (UMLS (ICD9CM) C0155649) =Disease or Syndrome
| - 2189. Acute poliomyelitis with other paralysis, poliovirus type II
- [ ] (UMLS (ICD9CM) C0152996) =Disease or Syndrome
|
- 2140. Acute myocardial infarction, of other lateral wall, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155650) =Disease or Syndrome
| - 2190. Acute poliomyelitis with other paralysis, poliovirus type III
- [ ] (UMLS (ICD9CM) C0152997) =Disease or Syndrome
|
- 2141. Acute myocardial infarction, of other specified sites
- [ ] (UMLS (ICD9CM) C0155659) =Disease or Syndrome
| - 2191. Acute poliomyelitis with other paralysis, unspecified type of poliovirus
- [ ] (UMLS (ICD9CM) C0152994) =Disease or Syndrome
|
- 2142. Acute myocardial infarction, of other specified sites, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155660) =Disease or Syndrome ;
| - 2192. ACUTE POST-THORACOT PAIN
- [ ] (UMLS (ICD9CM) C1719390) Acute post-thoracotomy pain =Disease or Syndrome ;
|
- 2143. Acute myocardial infarction, of other specified sites, initial episode of care
- [ ] (UMLS (ICD9CM) C0155661) =Disease or Syndrome ;
| - 2193. ACUTE POSTOP PAIN NEC
- [ ] (UMLS (ICD9CM) C1719392) Other acute postoperative pain =Disease or Syndrome ;
|
- 2144. Acute myocardial infarction, of other specified sites, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155662) =Disease or Syndrome ;
| - 2194. acute promyelocytic leukemia
- [A type of acute myeloid leukemia, a quickly progressing disease in which too many immature blood-forming cells are found in the blood and bone marrow. ( NCI )] (UMLS (CSP) C0023487) =Neoplastic Process =acute granulocytic leukemia;
|
- 2145. Acute myocardial infarction, subendocardial infarction
- [ ] (UMLS (ICD9CM) C0155655) =Disease or Syndrome
| - 2195. Acute Promyelocytic Leukemia with t(11;17)(q13;q21)
- (UMLS (NCI) C1332158) =Neoplastic Process ;
|
- 2146. Acute myocardial infarction, subendocardial infarction, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0494580) =Disease or Syndrome ;
| - 2196. Acute Promyelocytic Leukemia with t(11;17)(q23;q21)
- (UMLS (NCI) C1332159) =Neoplastic Process ;
|
- 2147. Acute myocardial infarction, subendocardial infarction, initial episode of care
- [ ] (UMLS (ICD9CM) C0155657) =Disease or Syndrome
| - 2197. Acute Promyelocytic Leukemia with t(15;17) (q22;q12)
- [A type of acute myeloid leukemia, a quickly progressing disease in which too many immature blood-forming cells are found in the blood and bone marrow. ( NCI )] (UMLS (NCI) C1332160) Acute Promyelocytic Leukemia with t(15;17)(q22;q12)(PML/RARa);
=Neoplastic Process ;
|
- 2148. Acute myocardial infarction, subendocardial infarction, subsequent episode of care
- [ ] (UMLS (ICD9CM) C0155658) =Disease or Syndrome
| - 2198. Acute Promyelocytic Leukemia with t(17;17)(q11;q11)
- (UMLS (NCI) C1510769) =Neoplastic Process ;
|
- 2149. Acute myocardial infarction, true posterior wall infarction
- [ ] (UMLS (ICD9CM) C0264706) =Disease or Syndrome
| - 2199. Acute Promyelocytic Leukemia with t(5;17)(q32;q12)
- (UMLS (NCI) C1332161) =Neoplastic Process ;
|
- 2150. Acute myocardial infarction, true posterior wall infarction, episode of care unspecified
- [ ] (UMLS (ICD9CM) C0155652) =Disease or Syndrome
| - 2200. Acute Promyelocytic Leukemia with Variant Translocations
- (UMLS (NCI) C1332157) =Neoplastic Process ;
|
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