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Pediatric Disease Annotations & Medicines



   acute myocarditis
  

Disease ID 981
Disease acute myocarditis
Definition
The sudden onset of inflammation of heart muscle with myocellular necrosis; this is generally secondary to an infectious cause, and patients often have a recent history of a flu-like illness.
Synonym
[x]acute myocarditis, unspecified
[x]acute myocarditis, unspecified (disorder)
acute myocarditis (disorder)
acute myocarditis nos
acute myocarditis nos (disorder)
acute myocarditis, nos
acute myocarditis, unspecified
acute myocarditis, unspecified (disorder)
myocarditis acute
DOID
ICD10
UMLS
C0155686
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0018801  |  heart failure  |  5
C0878544  |  cardiomyopathy  |  3
C0024537  |  vivax malaria  |  2
C0018801  |  cardiac failure  |  2
C0007193  |  dilated cardiomyopathy  |  2
C0009319  |  colitis  |  1
C0009324  |  ulcerative colitis  |  1
C0034063  |  pulmonary oedema  |  1
C1442837  |  myocardial necrosis  |  1
C0034063  |  pulmonary edema  |  1
C0030305  |  pancreatitis  |  1
C0014118  |  endocarditis  |  1
C0034065  |  pulmonary embolism  |  1
C0031039  |  pericardial effusion  |  1
C0019100  |  dengue hemorrhagic fever  |  1
C0023788  |  whipple's disease  |  1
C0004245  |  av block  |  1
C1565489  |  renal insufficiency  |  1
C0011849  |  diabetes mellitus  |  1
C0519030  |  klebsiella pneumonia  |  1
C0026691  |  kawasaki disease  |  1
C0008148  |  chlamydia  |  1
C0011847  |  diabetes  |  1
C0039483  |  giant cell arteritis  |  1
C0023364  |  leptospirosis  |  1
C0155626  |  acute myocardial infarction  |  1
C0008728  |  churg-strauss syndrome  |  1
C0398623  |  hypercoagulable state  |  1
C0013264  |  duchenne muscular dystrophy (dmd)  |  1
C0032285  |  pneumoniae  |  1
C0004245  |  atrioventricular block  |  1
C0085253  |  adult-onset still's disease  |  1
C0031046  |  pericarditis  |  1
C0042769  |  viral infection  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:107)
10344  |  CCL26  |  DISEASES
5318  |  PKP2  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
5008  |  OSM  |  DISEASES
51311  |  TLR8  |  DISEASES
2222  |  FDFT1  |  DISEASES
4741  |  NEFM  |  DISEASES
858  |  CAV2  |  DISEASES
944  |  TNFSF8  |  DISEASES
6347  |  CCL2  |  DISEASES
6783  |  SULT1E1  |  DISEASES
3565  |  IL4  |  DISEASES
27434  |  POLM  |  DISEASES
56829  |  ZC3HAV1  |  DISEASES
10647  |  SCGB1D2  |  DISEASES
8744  |  TNFSF9  |  DISEASES
970  |  CD70  |  DISEASES
968  |  CD68  |  DISEASES
3741  |  KCNA5  |  DISEASES
3958  |  LGALS3  |  DISEASES
1401  |  CRP  |  DISEASES
29958  |  DMGDH  |  DISEASES
3569  |  IL6  |  DISEASES
971  |  CD72  |  DISEASES
23316  |  CUX2  |  DISEASES
57017  |  COQ9  |  DISEASES
10552  |  ARPC1A  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
64135  |  IFIH1  |  DISEASES
10578  |  GNLY  |  DISEASES
943  |  TNFRSF8  |  DISEASES
941  |  CD80  |  DISEASES
3383  |  ICAM1  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
939  |  CD27  |  DISEASES
3001  |  GZMA  |  DISEASES
84651  |  SPINK7  |  DISEASES
138151  |  NACC2  |  DISEASES
133  |  ADM  |  DISEASES
1489  |  CTF1  |  DISEASES
7292  |  TNFSF4  |  DISEASES
23250  |  ATP11A  |  DISEASES
7547  |  ZIC3  |  DISEASES
1636  |  ACE  |  DISEASES
7412  |  VCAM1  |  DISEASES
5937  |  RBMS1  |  DISEASES
4880  |  NPPC  |  DISEASES
8320  |  EOMES  |  DISEASES
7098  |  TLR3  |  DISEASES
915  |  CD3D  |  DISEASES
1673  |  DEFB4A  |  DISEASES
3094  |  HINT1  |  DISEASES
121391  |  KRT74  |  DISEASES
344561  |  GPR148  |  DISEASES
836  |  CASP3  |  DISEASES
3728  |  JUP  |  DISEASES
11238  |  CA5B  |  DISEASES
1776  |  DNASE1L3  |  DISEASES
5551  |  PRF1  |  DISEASES
8824  |  CES2  |  DISEASES
2187  |  FANCB  |  DISEASES
942  |  CD86  |  DISEASES
3751  |  KCND2  |  DISEASES
115286  |  SLC25A26  |  DISEASES
1981  |  EIF4G1  |  DISEASES
7137  |  TNNI3  |  DISEASES
859  |  CAV3  |  DISEASES
7316  |  UBC  |  DISEASES
4624  |  MYH6  |  DISEASES
5169  |  ENPP3  |  DISEASES
1121  |  CHM  |  DISEASES
5094  |  PCBP2  |  DISEASES
1523  |  CUX1  |  DISEASES
919  |  CD247  |  DISEASES
9851  |  KIAA0753  |  DISEASES
7139  |  TNNT2  |  DISEASES
9447  |  AIM2  |  DISEASES
9531  |  BAG3  |  DISEASES
4923  |  NTSR1  |  DISEASES
959  |  CD40LG  |  DISEASES
1757  |  SARDH  |  DISEASES
958  |  CD40  |  DISEASES
7099  |  TLR4  |  DISEASES
7295  |  TXN  |  DISEASES
199  |  AIF1  |  DISEASES
4879  |  NPPB  |  DISEASES
3604  |  TNFRSF9  |  DISEASES
7293  |  TNFRSF4  |  DISEASES
3443  |  IFNA6  |  DISEASES
6194  |  RPS6  |  DISEASES
145270  |  PRIMA1  |  DISEASES
3122  |  HLA-DRA  |  DISEASES
3965  |  LGALS9  |  DISEASES
80380  |  PDCD1LG2  |  DISEASES
23210  |  JMJD6  |  DISEASES
7124  |  TNF  |  DISEASES
4615  |  MYD88  |  DISEASES
11155  |  LDB3  |  DISEASES
3586  |  IL10  |  DISEASES
30819  |  KCNIP2  |  DISEASES
3620  |  IDO1  |  DISEASES
3347  |  HTN3  |  DISEASES
7138  |  TNNT1  |  DISEASES
246734  |  NPCDR1  |  DISEASES
54938  |  SARS2  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 981
Disease acute myocarditis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:23)
HP:0000969  |  Dropsy  |  7
HP:0001635  |  Congestive heart failure  |  7
HP:0001638  |  Cardiomyopathy  |  3
HP:0030149  |  Cardiovascular shock  |  3
HP:0100749  |  Thoracic pain  |  2
HP:0012531  |  Pain  |  2
HP:0001644  |  Congestive cardiomyopathy  |  2
HP:0100598  |  Pulmonary oedema  |  2
HP:0100584  |  Endocarditis  |  1
HP:0012089  |  Arteritis  |  1
HP:0100279  |  Ulcerative colitis  |  1
HP:0001698  |  Pericardial effusions  |  1
HP:0005110  |  Atrial fibrillation  |  1
HP:0001701  |  Pericarditis  |  1
HP:0100571  |  Cardiac diverticulum  |  1
HP:0004308  |  Ventricular arrhythmia  |  1
HP:0001733  |  Pancreatic inflammation  |  1
HP:0001700  |  Myocardial necrosis  |  1
HP:0001678  |  Atrioventricular block  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0002583  |  Colitis  |  1
HP:0011675  |  Arrhythmias  |  1
Disease ID 981
Disease acute myocarditis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:22)
C2712322  |  tachycardia
C2216002  |  left posterior hemiblock
C2215935  |  complete heart block
C2108077  |  atrioventricular block
C1959587  |  ventricular free wall rupture
C1388902  |  asynergy
C1373218  |  immunosuppression
C1176537  |  influenza
C0519097  |  left ventricular aneurysm
C0264914  |  bifascicular block
C0205700  |  asymmetric septal hypertrophy
C0087086  |  thrombi
C0035400  |  reye's syndrome
C0030805  |  bullous pemphigoid
C0027051  |  myocardial infarction
C0024043  |  low t3 syndrome
C0018802  |  congestive heart failure
C0018801  |  heart failure
C0018801  |  cardiac failure
C0014145  |  yolk sac tumor
C0004245  |  atrioventricular heart block
C0000737  |  abdominal pain
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0018801  |  heart failure  |  5
C0018801  |  cardiac failure  |  2
C0004245  |  atrioventricular block  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)