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1201. Acute gastric ulcer with hemorrhage and perforation
[ ] (UMLS (ICD9CM) C0155973) =Disease or Syndrome
1251. Acute Myelofibrosis
[An acute myeloid leukemia characterized by bone marrow fibrosis. The prognosis is usually poor. (WHO, 2001) ( NCI )] (UMLS (NCI) C0334674) =Neoplastic Process
1202. Acute gastric ulcer with perforation
[ ] (UMLS (ICD9CM) C0155970) =Disease or Syndrome ;
1252. 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 ;
1203. Acute gastric ulcer without mention of hemorrhage or perforation
[ ] (UMLS (ICD9CM) C0267124) =Disease or Syndrome ;
1253. 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
1204. Acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction
[ ] (UMLS (ICD9CM) C0267125) =Disease or Syndrome ;
1254. 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 ;
1205. Acute gastritis
(UMLS (ICD9CM) C0149518) =Disease or Syndrome
1255. 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
1206. ACUTE GASTRITIS W HMRHG
[ ] (UMLS (ICD9CM) C0267112) =Disease or Syndrome ;
1256. 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
1207. Acute gastritis, without mention of hemorrhage
[ ] (UMLS (ICD9CM) C0156070) =Disease or Syndrome
1257. 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 ;
1208. Acute gastrojejunal ulcer with hemorrhage
[ ] (UMLS (ICD9CM) C0156042) =Disease or Syndrome ;
1258. 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
1209. Acute gastrojejunal ulcer with hemorrhage and perforation
[ ] (UMLS (ICD9CM) C0156048) =Disease or Syndrome ;
1259. 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 ;
1210. Acute gastrojejunal ulcer with perforation
[ ] (UMLS (ICD9CM) C0156045) =Disease or Syndrome ;
1260. 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
1211. Acute gastrojejunal ulcer without mention of hemorrhage or perforation
[ ] (UMLS (ICD9CM) C0392501) =Acquired Abnormality; Disease or Syndrome ;
1261. Acute Myeloid Leukemia with t(16;16)(p13;q22)
(UMLS (NCI) C1332155) Acute Myeloid Leukemia, t(16;16)(p13;q22);
=Neoplastic Process ;
1212. ACUTE GC INFECT LOWER GU
(UMLS (ICD9CM) C0018074) =Disease or Syndrome
1262. 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
1213. ACUTE GC SALPINGITIS
[ ] (UMLS (ICD9CM) C0275654) =Disease or Syndrome
1263. 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 ;
1214. ACUTE GINGITITIS, PLAQUE
[ ] (UMLS (ICD9CM) C1719490) Acute gingivitis, plaque induced =Disease or Syndrome
1264. 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 ;
1215. Acute gingivitis
[ ] (UMLS (ICD9CM) C0155937) =Disease or Syndrome ;
1265. Acute Myelomonocytic Leukemia in Remission
(UMLS (NCI) C0836973) =Neoplastic Process
1216. Acute glomerulonephritis
[ ] (UMLS (ICD9CM) C0156221) =Disease or Syndrome
1266. Acute Myelomonocytic Leukemia with Abnormal Eosinophils
(UMLS (NCI) C1332156) AMML Eo;
FAB M4Eo =Neoplastic Process ;
1217. Acute glomerulonephritis with other specified pathological lesion in kidney
[ ] (UMLS (ICD9CM) C0156224) =Disease or Syndrome
1267. 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
1218. Acute glomerulonephritis with unspecified pathological lesion in kidney
[ ] (UMLS (ICD9CM) C0156226) =Disease or Syndrome
1268. Acute myocardial infarction, of anterolateral wall
[ ] (UMLS (ICD9CM) C0155627) =Disease or Syndrome
1219. Acute Gonococcal Infection of Upper Genitourinary Tract
(UMLS (NCI) C0375028) =Disease or Syndrome
1269. Acute myocardial infarction, of anterolateral wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155628) =Disease or Syndrome
1220. Acute Graft Versus Host Disease
[A syndrome of immologically mediated tissue damage occurring following allogeneic transplant usually affecting the skin, liver, and gi tract. Onset is usually within one hundred days of transplantation or immunologic manipulation. ( NCI )] (UMLS (NCI) C0856825) Acute GVHD;
Fulminant Graft Versus Host Disease;
=Disease or Syndrome
1270. Acute myocardial infarction, of anterolateral wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155629) =Disease or Syndrome
1221. acute granulocytic leukemia
[acute leukemia arising from myeloid tissue in which the granular, polymorphonuclear leukocytes and their precursors predominate. ( CSP )] (UMLS (CSP) C0023467) =Neoplastic Process =acute granulocytic leukemia;
granulocytic leukemia;
Acute Leukemia;
=Acute Basophilic Leukemia;
Acute Eosinophilic Leukemia;
Acute Erythroblastic Leukemia;
Leukemia, Mast-Cell;
Acute M7 Myeloid Leukemia;
acute monoblastic leukemia;
acute granulocytic leukemia;
acute promyelocytic leukemia;
1271. Acute myocardial infarction, of anterolateral wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155630) =Disease or Syndrome
1222. Acute Hemolytic Transfusion Reaction
(UMLS (HL7) C1549006) =Pathologic Function =Transfusion Adverse Reaction;
1272. Acute myocardial infarction, of inferolateral wall
[ ] (UMLS (ICD9CM) C0340308) =Disease or Syndrome
1223. Acute Hemorrhagic Conjunctivitis
[A highly contagious disease characterized by subconjunctival hemorrhage, sudden swelling of the eyelids and congestion, redness, and pain in the eye. Epidemic conjunctivitis caused by Enterovirus 70 (EV-70) was first described in Africa in 1969. It is caused also by Coxsackievirus A24 variant (CA24v). Epidemics by this organism have appeared most frequently in Asia. ( MSH )] (UMLS (NCI) C0009765) =Disease or Syndrome =Conjunctivitis, Viral;
Coxsackievirus Infections
1273. Acute myocardial infarction, of inferolateral wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155636) =Disease or Syndrome
1224. Acute Hemorrhagic Encephalitis
(UMLS (NCI) C1332149) =Disease or Syndrome ;
1274. Acute myocardial infarction, of inferolateral wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155637) =Disease or Syndrome
1225. Acute Hepatitis
(UMLS (NCI) C0267797) =Disease or Syndrome ;
1275. Acute myocardial infarction, of inferolateral wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155638) =Disease or Syndrome
1226. Acute hepatitis C with hepatic coma
[ ] (UMLS (ICD9CM) C1456261) HPT C ACUTE W HEPAT COMA;
=Disease or Syndrome
1276. Acute myocardial infarction, of inferoposterior wall
[ ] (UMLS (ICD9CM) C0340304) =Disease or Syndrome
1227. Acute hepatitis C without mention of hepatic coma
[ ] (UMLS (ICD9CM) C1456262) HPT C ACUTE WO HPAT COMA;
=Disease or Syndrome
1277. Acute myocardial infarction, of inferoposterior wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155640) =Disease or Syndrome
1228. ACUTE INFECTION OF PINNA
[ ] (UMLS (ICD9CM) C0155392) =Disease or Syndrome
1278. Acute myocardial infarction, of inferoposterior wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155641) =Disease or Syndrome
1229. acute infectious nonbacterial gastroenteritis
[epidemic, highly communicable disease of sudden onset, caused by the epidemic gastroenteritis virus (especially Norwalk agent) which affects all age groups; infection is associated with fever, abdominal cramps, nausea, vomiting, diarrhea, and headache, one or another of which may be predominant. ( CSP )] (UMLS (CSP) C1306859) =Disease or Syndrome ;
=Gastrointestinal Infection;
1279. Acute myocardial infarction, of inferoposterior wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155642) =Disease or Syndrome
1230. ACUTE INFLAM NOS, ORBIT
[ ] (UMLS (ICD9CM) C0155256) =Disease or Syndrome ;
1280. Acute myocardial infarction, of other anterior wall
[ ] (UMLS (ICD9CM) C0155631) =Disease or Syndrome
1231. Acute Inflammatory Infiltrate
(UMLS (NCI) C0333361) =Finding
1281. Acute myocardial infarction, of other anterior wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155632) =Disease or Syndrome
1232. acute intermittent porphyria
[An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine. ( MSH )] (UMLS (CSP) C0162565) =Disease or Syndrome ;
=Porphyria, Hepatic;
1282. Acute myocardial infarction, of other anterior wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155633) =Disease or Syndrome
1233. Acute Interstitial Pneumonia
(UMLS (NCI) C1279945) Acute Interstitial Pneumonitis;
AIP =Disease or Syndrome
1283. Acute myocardial infarction, of other anterior wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155634) =Disease or Syndrome
1234. Acute laryngitis
(UMLS (ICD9CM) C0001327) =Disease or Syndrome ;
1284. Acute myocardial infarction, of other inferior wall
[ ] (UMLS (ICD9CM) C0155643) =Disease or Syndrome
1235. Acute laryngitis/tracheitis
(UMLS (ICPC) C0155811) (Acute laryngitis/tracheitis; LARINGITI ZORROTZA/ TRAKETITIA/ DIFTERIA; Akut laryngit/trakeit/strubehoste; Acute laryngitis/tracheitis; AKUUTTI KURKUNPAAN TULEHDUS,LARYNGIITTI/TRAKEIITTI; Laryngite aigue/tracheite aigue; akute Laryngitis/Tracheitis; laringitis xarifa; (119); Laringite acuta/tracheite; AKUTT LARYNGITT/TRAKEITT/KRUPP; Laringite/traqueite aguda/crupe; Laringitis/traqueitis/crup agudo; AKUT LARYNGIT/TRAKEIT) Acute laryngitis/tracheitis =Disease or Syndrome ;
=Diagnosis/Diseases Component; Respiratory
1285. Acute myocardial infarction, of other inferior wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155644) =Disease or Syndrome
1236. ACUTE LARYNGOPHARYNGITIS
[ ] (UMLS (ICD9CM) C0155817) =Disease or Syndrome
1286. Acute myocardial infarction, of other inferior wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155645) =Disease or Syndrome
1237. acute laryngotracheobronchitis virus
[virus isolated from patients with acute laryngotracheobronchitis; causes febrile respiratory illness. ( CSP )] (UMLS (CSP) C0030391) =Virus ;
=paramyxovirus;
1287. Acute myocardial infarction, of other inferior wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155646) =Disease or Syndrome
1238. Acute Leukemia
[leukemia in which the involved cell shows little or no differentiation, usually consisting of blast cells; two types are distinguished, acute lymphocytic and acute myelogenous leukemia. ( CSP )] (UMLS (NCI) C0085669) =Neoplastic Process =Blood (Leukemia);
=acute lymphatic leukemia;
acute granulocytic leukemia;
1288. Acute myocardial infarction, of other lateral wall
[ ] (UMLS (ICD9CM) C0155647) =Disease or Syndrome
1239. Acute Leukemia of Ambiguous Lineage
[An acute leukemia in which the blasts lack sufficient evidence to classify as myeloid or lymphoid or they have morphologic and/or immunophenotypic characteristics of both myeloid and lymphoid cells. The prognosis is usually unfavorable. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C1301357) Acute Leukemia of Indeterminate Lineage;
Mixed-Cell Leukemia;
=Neoplastic Process
1289. Acute myocardial infarction, of other lateral wall, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155648) =Disease or Syndrome
1240. Acute lymphadenitis
(UMLS (ICPC) C0157705) (Acute lymphadenitis; LINFADENITIS ZORROTZA; Akut lymfadenit; Acute lymphadenitis; AKILLINEN IMUSOLMUKETULEHDUS; Lymphangite aigue; akute Lymphadenitis; limfadenitis xarifa; lymphadenitis acuta; Linfoadenite acuta; AKUTT LYMFADENITT; Linfadenite aguda; Linfadenitis aguda; AKUT LYMFKORTELSVULLNAD) Acute lymphadenitis =Disease or Syndrome =BLOOD, BLOOD FORMING ORGANS, LYMPHATICS, SPLEEN; Diagnosis/Diseases Component
1290. Acute myocardial infarction, of other lateral wall, initial episode of care
[ ] (UMLS (ICD9CM) C0155649) =Disease or Syndrome
1241. acute lymphatic leukemia
[acute leukemia in which lymphoblasts and their progenitor cells predominate; the most common childhood cancer and accounts for 20 percent of adult acute leukemia; common ALL antigen (CALLA) expressed in most cases. ( CSP )] (UMLS (CSP) C0023449) =Neoplastic Process ;
=Leukemia, Lymphocytic;
Acute Leukemia =Acute B Cell Lymphocytic Leukemia;
cALLa Positive Lymphoblastic Leukemia;
Childhood Acute Lymphoblastic Leukemia;
FAB L2;
Acute Biphenotypic Leukemia;
Leukemia, Null-Cell;
acute T cell leukemia;
1291. Acute myocardial infarction, of other lateral wall, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155650) =Disease or Syndrome
1242. Acute M4 Myeloid Leukemia
[An acute leukemia characterized by the proliferation of both neutrophil and monocyte precursors. Patients typically present with anemia, thrombocytopenia, fever and fatigue. This type of leukemia frequently responds to aggressive therapy. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C0023479) =Neoplastic Process =granulocytic leukemia;
1292. Acute myocardial infarction, of other specified sites
[ ] (UMLS (ICD9CM) C0155659) =Disease or Syndrome
1243. Acute M7 Myeloid Leukemia
[An acute myeloid leukemia in which at least 50% of the blasts are of megakaryocytic lineage. The prognosis is usually poor. (WHO, 2001) ( NCI )] (UMLS (NCI) C0023462) =Neoplastic Process =acute granulocytic leukemia;
1293. Acute myocardial infarction, of other specified sites, episode of care unspecified
[ ] (UMLS (ICD9CM) C0155660) =Disease or Syndrome ;
1244. Acute mastoiditis
[ ] (UMLS (ICD9CM) C0701825) =Disease or Syndrome
1294. Acute myocardial infarction, of other specified sites, initial episode of care
[ ] (UMLS (ICD9CM) C0155661) =Disease or Syndrome ;
1245. ACUTE MILIARY TB-CULT DX
[ ] (UMLS (ICD9CM) C0152919) =Disease or Syndrome
1295. Acute myocardial infarction, of other specified sites, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155662) =Disease or Syndrome ;
1246. ACUTE MILIARY TB-NO EXAM
[ ] (UMLS (ICD9CM) C0152916) =Disease or Syndrome
1296. Acute myocardial infarction, subendocardial infarction
[ ] (UMLS (ICD9CM) C0155655) =Disease or Syndrome
1247. acute monoblastic leukemia
[uncommon form of acute myelogenous leukemia, in which the predominating cells are identified as monocytes; a few myelocytes may be present, but not as many as in acute myelomonocytic leukemia. ( CSP )] (UMLS (CSP) C0023465) =Neoplastic Process =Histiocytic Disorders, Malignant;
Blood (Leukemia);
acute granulocytic leukemia;
1297. Acute myocardial infarction, subendocardial infarction, episode of care unspecified
[ ] (UMLS (ICD9CM) C0494580) =Disease or Syndrome ;
1248. Acute Monoblastic Leukemia
[An acute myeloid leukemia in which the monoblasts represent 80% or more of the total cellular population. (WHO, 2001) — 2003 ( NCI )] (UMLS (NCI) C0457334) =Neoplastic Process
1298. Acute myocardial infarction, subendocardial infarction, initial episode of care
[ ] (UMLS (ICD9CM) C0155657) =Disease or Syndrome
1249. Acute Monocytic Leukemia
[An acute myeloid leukemia in which the majority of monocytic cells are promonocytes. (WHO, 2001) ( NCI )] (UMLS (NCI) C1318544) Acute Monocytic Leukemia (FAB M5b);
=Neoplastic Process
1299. Acute myocardial infarction, subendocardial infarction, subsequent episode of care
[ ] (UMLS (ICD9CM) C0155658) =Disease or Syndrome
1250. Acute Myeloblastic Leukemia with Minimal Differentiation
[An acute myeloid leukemia (AML) in which the blasts do not show evidence of myeloid differentiation by morphology and conventional cytochemistry. The myeloid origin of the blasts is demonstrated by immunohistochemistry and/or electron microscopic studies. The patients present with anemia, neutropenia, and thrombocytopenia. The prognosis is usually poor. (WHO, 2001) ( NCI )] (UMLS (NCI) C0522631) =Neoplastic Process
1300. Acute myocardial infarction, true posterior wall infarction
[ ] (UMLS (ICD9CM) C0264706) =Disease or Syndrome

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