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Pediatric Disease Annotations & Medicines



   acute chest syndrome
  

Disease ID 1584
Disease acute chest syndrome
Definition
Respiratory syndrome characterized by the appearance of a new pulmonary infiltrate on chest x-ray, accompanied by symptoms of fever, cough, chest pain, tachypnea, or DYSPNEA, often seen in patients with SICKLE CELL ANEMIA. Multiple factors (e.g., infection, and pulmonary FAT EMBOLISM) may contribute to the development of the syndrome.
Synonym
acute chest syndrome (disorder)
acute chest syndrome [disease/finding]
acute chest syndrome in sickle cell disease
acute chest syndromes
syndrome, acute chest
syndromes, acute chest
DOID
UMLS
C0742343
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:13)
C0002895  |  sickle cell disease  |  21
C0002871  |  anemia  |  3
C0002895  |  sickle cell anemia  |  3
C0040053  |  thrombosis  |  2
C0004096  |  asthma  |  2
C0037054  |  sickle cell trait  |  1
C0002895  |  sickle cell anaemia  |  1
C0007785  |  cerebral infarct  |  1
C0007785  |  cerebral infarcts  |  1
C1145670  |  respiratory failure  |  1
C0032285  |  pneumonia  |  1
C0002871  |  anaemia  |  1
C0238425  |  sickle cell crisis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:63)
7049  |  TGFBR3  |  DISEASES
420  |  ART4  |  DISEASES
56920  |  SEMA3G  |  DISEASES
391013  |  PLA2G2C  |  DISEASES
2952  |  GSTT1  |  DISEASES
3040  |  HBA2  |  DISEASES
3685  |  ITGAV  |  DISEASES
7450  |  VWF  |  DISEASES
6403  |  SELP  |  DISEASES
55850  |  USE1  |  DISEASES
3263  |  HPX  |  DISEASES
8128  |  ST8SIA2  |  DISEASES
149951  |  COMMD7  |  DISEASES
6326  |  SCN2A  |  DISEASES
1636  |  ACE  |  DISEASES
114757  |  CYGB  |  DISEASES
6006  |  RHCE  |  DISEASES
7412  |  VCAM1  |  DISEASES
23305  |  ACSL6  |  DISEASES
4846  |  NOS3  |  DISEASES
5724  |  PTAFR  |  DISEASES
51282  |  SCAND1  |  DISEASES
375611  |  SLC26A5  |  DISEASES
2944  |  GSTM1  |  DISEASES
5319  |  PLA2G1B  |  DISEASES
151516  |  ASPRV1  |  DISEASES
6764  |  ST5  |  DISEASES
3039  |  HBA1  |  DISEASES
3047  |  HBG1  |  DISEASES
3043  |  HBB  |  DISEASES
9138  |  ARHGEF1  |  DISEASES
3048  |  HBG2  |  DISEASES
3266  |  ERAS  |  DISEASES
7137  |  TNNI3  |  DISEASES
3792  |  KEL  |  DISEASES
51703  |  ACSL5  |  DISEASES
5725  |  PTBP1  |  DISEASES
1201  |  CLN3  |  DISEASES
2993  |  GYPA  |  DISEASES
7855  |  FZD5  |  DISEASES
5742  |  PTGS1  |  DISEASES
58  |  ACTA1  |  DISEASES
28514  |  DLL1  |  DISEASES
383  |  ARG1  |  DISEASES
959  |  CD40LG  |  DISEASES
953  |  ENTPD1  |  DISEASES
11093  |  ADAMTS13  |  DISEASES
55315  |  SLC29A3  |  DISEASES
7099  |  TLR4  |  DISEASES
9966  |  TNFSF15  |  DISEASES
5320  |  PLA2G2A  |  DISEASES
8858  |  PROZ  |  DISEASES
57704  |  GBA2  |  DISEASES
1906  |  EDN1  |  DISEASES
3045  |  HBD  |  DISEASES
83650  |  SLC35G5  |  DISEASES
8399  |  PLA2G10  |  DISEASES
720  |  C4A  |  DISEASES
58155  |  PTBP2  |  DISEASES
80012  |  PHC3  |  DISEASES
2533  |  FYB  |  DISEASES
64426  |  SUDS3  |  DISEASES
5228  |  PGF  |  DISEASES
Locus(Waiting for update.)
Disease ID 1584
Disease acute chest syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:9)
HP:0001903  |  Anemia  |  4
HP:0002099  |  Asthma  |  2
HP:0002090  |  Pneumonia  |  1
HP:0030828  |  Wheezing  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0100750  |  Pulmonary atelectasis  |  1
HP:0012531  |  Pain  |  1
HP:0002878  |  Respiratory failure  |  1
HP:0012418  |  Low blood oxygen level  |  1
Disease ID 1584
Disease acute chest syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs41322052173519274846NOS3umls:C0742343BeFreeNo associations were found between the genotype of the NOS3 T-786C SNP and ACS.0.0008143262007NOS37150993018CT
rs41322052146870364846NOS3umls:C0742343BeFreeAssociation of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease.0.0008143262004NOS37150993018CT
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0742343morphineD00902057-27-2acute chest syndromeMESH:D056586marker/mechanism15001964
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)