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Pediatric Disease Annotations & Medicines



   systolic heart failure
  

Disease ID 1051
Disease systolic heart failure
Definition
Heart failure caused by abnormal myocardial contraction during SYSTOLE leading to defective cardiac emptying.
Synonym
failure heart systolic
heart failure systolic
heart failure, systolic
heart failure, systolic [disease/finding]
heart failures, systolic
systolic heart failure (disorder)
systolic heart failure, unspecified
systolic heart failures
systolic hrt failure nos
DOID
UMLS
C1135191
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0022116  |  ischemia  |  3
C0002871  |  anemia  |  3
C0018801  |  heart failure  |  2
C0028754  |  obesity  |  2
C0018799  |  heart disease  |  2
C0878544  |  cardiomyopathy  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C0264832  |  peripartum cardiomyopathy  |  1
C0151744  |  myocardial ischemia  |  1
C0033953  |  sexual dysfunction  |  1
C1565489  |  renal insufficiency  |  1
C0155626  |  acute myocardial infarction  |  1
C0027051  |  myocardial infarction (mi)  |  1
C0010068  |  coronary artery disease  |  1
C0020542  |  pulmonary hypertension  |  1
C0242350  |  erectile dysfunction  |  1
C1135196  |  diastolic heart failure  |  1
C0011847  |  diabetes  |  1
C0520680  |  central sleep apnea  |  1
C0020538  |  hypertension  |  1
C0600260  |  obstructive pulmonary disease  |  1
C0024117  |  chronic obstructive pulmonary disease (copd)  |  1
C0026266  |  mitral regurgitation  |  1
C0024115  |  pulmonary disease  |  1
C0392077  |  cardiac sarcoidosis  |  1
C0011570  |  depression  |  1
C0027051  |  myocardial infarct  |  1
C0041696  |  major depression  |  1
C0037315  |  sleep apnea  |  1
C0027051  |  myocardial infarction  |  1
C0003507  |  aortic valve stenosis  |  1
C0019061  |  hemolytic uremic syndrome  |  1
C0006625  |  cachectic  |  1
C0024117  |  chronic obstructive pulmonary disease  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:4)
1636  |  ACE  |  infer
183  |  AGT  |  infer
4313  |  MMP2  |  infer
4879  |  NPPB  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:90)
5166  |  PDK4  |  DISEASES
54432  |  YIPF1  |  DISEASES
10278  |  EFS  |  DISEASES
7076  |  TIMP1  |  DISEASES
4313  |  MMP2  |  DISEASES
6822  |  SULT2A1  |  DISEASES
4353  |  MPO  |  DISEASES
9896  |  FIG4  |  DISEASES
8074  |  FGF23  |  DISEASES
7291  |  TWIST1  |  DISEASES
2069  |  EREG  |  DISEASES
583  |  BBS2  |  DISEASES
6945  |  MLX  |  DISEASES
1215  |  CMA1  |  DISEASES
59272  |  ACE2  |  DISEASES
9518  |  GDF15  |  DISEASES
3958  |  LGALS3  |  DISEASES
5989  |  RFX1  |  DISEASES
1401  |  CRP  |  DISEASES
10955  |  SERINC3  |  DISEASES
3569  |  IL6  |  DISEASES
4481  |  MSR1  |  DISEASES
6521  |  SLC4A1  |  DISEASES
23530  |  NNT  |  DISEASES
10058  |  ABCB6  |  DISEASES
1119  |  CHKA  |  DISEASES
7168  |  TPM1  |  DISEASES
2627  |  GATA6  |  DISEASES
5972  |  REN  |  DISEASES
185  |  AGTR1  |  DISEASES
10699  |  CORIN  |  DISEASES
3934  |  LCN2  |  DISEASES
133  |  ADM  |  DISEASES
1360  |  CPB1  |  DISEASES
9320  |  TRIP12  |  DISEASES
23576  |  DDAH1  |  DISEASES
23118  |  TAB2  |  DISEASES
7547  |  ZIC3  |  DISEASES
22808  |  MRAS  |  DISEASES
909  |  CD1A  |  DISEASES
1636  |  ACE  |  DISEASES
90525  |  SHF  |  DISEASES
11167  |  FSTL1  |  DISEASES
213  |  ALB  |  DISEASES
7349  |  UCN  |  DISEASES
4846  |  NOS3  |  DISEASES
11079  |  RER1  |  DISEASES
27129  |  HSPB7  |  DISEASES
8557  |  TCAP  |  DISEASES
23047  |  PDS5B  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
4312  |  MMP1  |  DISEASES
199699  |  DAND5  |  DISEASES
1585  |  CYP11B2  |  DISEASES
3665  |  IRF7  |  DISEASES
2192  |  FBLN1  |  DISEASES
6401  |  SELE  |  DISEASES
2626  |  GATA4  |  DISEASES
4306  |  NR3C2  |  DISEASES
2066  |  ERBB4  |  DISEASES
7273  |  TTN  |  DISEASES
875  |  CBS  |  DISEASES
8654  |  PDE5A  |  DISEASES
3084  |  NRG1  |  DISEASES
387129  |  NPSR1  |  DISEASES
4311  |  MME  |  DISEASES
1565  |  CYP2D6  |  DISEASES
183  |  AGT  |  DISEASES
7139  |  TNNT2  |  DISEASES
4720  |  NDUFS2  |  DISEASES
9531  |  BAG3  |  DISEASES
153  |  ADRB1  |  DISEASES
8277  |  TKTL1  |  DISEASES
4318  |  MMP9  |  DISEASES
84676  |  TRIM63  |  DISEASES
23564  |  DDAH2  |  DISEASES
4879  |  NPPB  |  DISEASES
4878  |  NPPA  |  DISEASES
1471  |  CST3  |  DISEASES
1906  |  EDN1  |  DISEASES
551  |  AVP  |  DISEASES
55835  |  CENPJ  |  DISEASES
2869  |  GRK5  |  DISEASES
136319  |  MTPN  |  DISEASES
79924  |  ADM2  |  DISEASES
1638  |  DCT  |  DISEASES
7124  |  TNF  |  DISEASES
2081  |  ERN1  |  DISEASES
8833  |  GMPS  |  DISEASES
10189  |  ALYREF  |  DISEASES
Locus(Waiting for update.)
Disease ID 1051
Disease systolic heart failure
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:33)
HP:0003546  |  Exercise intolerance  |  3
HP:0004308  |  Ventricular arrhythmia  |  3
HP:0001685  |  Myocardial fibrosis  |  3
HP:0005110  |  Atrial fibrillation  |  3
HP:0001903  |  Anemia  |  3
HP:0011675  |  Arrhythmias  |  3
HP:0001635  |  Congestive heart failure  |  2
HP:0001513  |  Obesity  |  2
HP:0001297  |  Cerebral vascular events  |  2
HP:0010536  |  Central sleep apnoea  |  1
HP:0000822  |  Hypertension  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0005575  |  Hemolytic-uremic syndrome  |  1
HP:0011106  |  Depleted blood volume  |  1
HP:0001645  |  Sudden cardiac death  |  1
HP:0000716  |  Depression  |  1
HP:0002104  |  Absence of spontaneous respiration  |  1
HP:0001681  |  Angina pectoris  |  1
HP:0002092  |  Pulmonary artery hypertension  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0002119  |  Ventricular dilatation  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0001653  |  Mitral valve insufficiency  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0001649  |  Tachycardia  |  1
HP:0000802  |  Erectile dysfunction  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0012664  |  Reduced ejection fraction  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0003073  |  Hypoalbuminaemia  |  1
HP:0001658  |  Myocardial infarction  |  1
HP:0006510  |  Chronic obstructive pulmonary disease  |  1
HP:0001714  |  Ventricular hypertrophy  |  1
Disease ID 1051
Disease systolic heart failure
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0232197  |  fibrillation  |  3
C1561644  |  chronic kidney disease (ckd)  |  1
C0041696  |  major depression  |  1
C0037315  |  sleep apnea  |  1
C0242350  |  erectile dysfunction  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1799998186385951585CYP11B2umls:C1135191BeFreeWe analyzed the possible association between aldosterone synthase (CYP11B2) T-344C polymorphism, which is associated with increased aldosterone activity, and the prevalence of atrial fibrillation (AF) in 196 consecutive patients who had symptomatic systolic heart failure (HF; left ventricular ejection fraction <40%) for > or =3 months before recruitment.0.0002714422008CYP11B2;LOC1053757938142918184AG
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
C1135191cyclophosphamideD00352050-18-0heart failure, systolicMESH:D054143marker/mechanism18462404
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)