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Pediatric Disease Annotations & Medicines



   sick sinus syndrome
  

Disease ID 154
Disease sick sinus syndrome
Definition
A condition caused by dysfunctions related to the SINOATRIAL NODE including impulse generation (CARDIAC SINUS ARREST) and impulse conduction (SINOATRIAL EXIT BLOCK). It is characterized by persistent BRADYCARDIA, chronic ATRIAL FIBRILLATION, and failure to resume sinus rhythm following CARDIOVERSION. This syndrome can be congenital or acquired, particularly after surgical correction for heart defects.
Synonym
sick sinus node syndrome
sick sinus syndrome (disorder)
sick sinus syndrome [disease/finding]
sick syndrome sinus
sinus sick syndrome
sss
syndrome sick sinus
syndrome, sick sinus
DOID
ICD10
UMLS
C0037052
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:18)
C0037052  |  sick sinus syndrome  |  24
C0004245  |  atrioventricular block  |  2
C0043119  |  werner's syndrome  |  1
C0152021  |  congenital heart disease  |  1
C0002395  |  alzheimer's disease  |  1
C0018801  |  heart failure  |  1
C0042373  |  vascular disease  |  1
C0018799  |  heart disease  |  1
C0011847  |  diabetes  |  1
C0026896  |  myasthenia gravis  |  1
C0007131  |  nsclc  |  1
C0011849  |  diabetes mellitus  |  1
C0037315  |  sleep apnea  |  1
C0007222  |  cardiovascular disease  |  1
C1142166  |  brugada syndrome  |  1
C0520679  |  obstructive sleep apnea  |  1
C0004245  |  av block  |  1
C0023801  |  lipomatosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:4)
POMC  |  5443  |  CTD_human
HCN4  |  10021  |  ORPHANET;GHR
MYH6  |  4624  |  CTD_human;ORPHANET;GHR
SCN5A  |  6331  |  CLINVAR;ORPHANET;GHR
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
3760  |  KCNJ3  |  infer
3762  |  KCNJ5  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:86)
79176  |  FBXL15  |  DISEASES
1594  |  CYP27B1  |  DISEASES
55856  |  ACOT13  |  DISEASES
3670  |  ISL1  |  DISEASES
7291  |  TWIST1  |  DISEASES
84329  |  HVCN1  |  DISEASES
55154  |  MSTO1  |  DISEASES
6945  |  MLX  |  DISEASES
54795  |  TRPM4  |  DISEASES
6737  |  TRIM21  |  DISEASES
759  |  CA1  |  DISEASES
6926  |  TBX3  |  DISEASES
6741  |  SSB  |  DISEASES
10060  |  ABCC9  |  DISEASES
10021  |  HCN4  |  DISEASES
22858  |  ICK  |  DISEASES
7112  |  TMPO  |  DISEASES
3073  |  HEXA  |  DISEASES
2702  |  GJA5  |  DISEASES
138151  |  NACC2  |  DISEASES
5805  |  PTS  |  DISEASES
2697  |  GJA1  |  DISEASES
55364  |  IMPACT  |  DISEASES
7547  |  ZIC3  |  DISEASES
51422  |  PRKAG2  |  DISEASES
909  |  CD1A  |  DISEASES
9992  |  KCNE2  |  DISEASES
3046  |  HBE1  |  DISEASES
8841  |  HDAC3  |  DISEASES
5308  |  PITX2  |  DISEASES
2147  |  F2  |  DISEASES
6910  |  TBX5  |  DISEASES
8884  |  SLC5A6  |  DISEASES
11238  |  CA5B  |  DISEASES
124590  |  USH1G  |  DISEASES
8289  |  ARID1A  |  DISEASES
1827  |  RCAN1  |  DISEASES
78987  |  CRELD1  |  DISEASES
1482  |  NKX2-5  |  DISEASES
3739  |  KCNA4  |  DISEASES
6331  |  SCN5A  |  DISEASES
10231  |  RCAN2  |  DISEASES
2626  |  GATA4  |  DISEASES
51337  |  THEM6  |  DISEASES
859  |  CAV3  |  DISEASES
9536  |  PTGES  |  DISEASES
165904  |  XIRP1  |  DISEASES
7273  |  TTN  |  DISEASES
4635  |  MYL4  |  DISEASES
4624  |  MYH6  |  DISEASES
287  |  ANK2  |  DISEASES
26151  |  NAT9  |  DISEASES
2764  |  GMFB  |  DISEASES
51592  |  TRIM33  |  DISEASES
8913  |  CACNA1G  |  DISEASES
147409  |  DSG4  |  DISEASES
1201  |  CLN3  |  DISEASES
4514  |  MT-CO3  |  DISEASES
4537  |  MT-ND3  |  DISEASES
6262  |  RYR2  |  DISEASES
383  |  ARG1  |  DISEASES
3766  |  KCNJ10  |  DISEASES
57657  |  HCN3  |  DISEASES
10654  |  PMVK  |  DISEASES
85413  |  SLC22A16  |  DISEASES
9096  |  TBX18  |  DISEASES
84890  |  ADO  |  DISEASES
4303  |  FOXO4  |  DISEASES
23564  |  DDAH2  |  DISEASES
3055  |  HCK  |  DISEASES
5420  |  PODXL  |  DISEASES
1832  |  DSP  |  DISEASES
8502  |  PKP4  |  DISEASES
3776  |  KCNK2  |  DISEASES
5999  |  RGS4  |  DISEASES
6474  |  SHOX2  |  DISEASES
11155  |  LDB3  |  DISEASES
4152  |  MBD1  |  DISEASES
374308  |  PTCHD3  |  DISEASES
142891  |  SAMD8  |  DISEASES
4607  |  MYBPC3  |  DISEASES
5053  |  PAH  |  DISEASES
9628  |  RGS6  |  DISEASES
378938  |  MALAT1  |  DISEASES
104564225  |  MHRT  |  DISEASES
103752588  |  PACERR  |  DISEASES
Locus(Waiting for update.)
Disease ID 154
Disease sick sinus syndrome
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:20)
Disease ID 154
Disease sick sinus syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:30)
C2720186  |  atrial standstill
C2712322  |  tachycardia
C2697375  |  brugada syndrome
C2242664  |  lipomatous hypertrophy of the interatrial septum
C2108093  |  paroxysmal supraventricular tachycardia
C2041142  |  left bundle branch block
C1550639  |  fistula
C1414542  |  marfan syndrome
C0694539  |  chronic atrial fibrillation
C0520679  |  obstructive sleep apnea syndrome
C0428908  |  sinus node dysfunction
C0345138  |  pericardial defect
C0264886  |  conduction defects
C0235480  |  paroxysmal atrial fibrillation
C0234435  |  cough syncope
C0232197  |  fibrillation
C0206138  |  crest syndrome
C0042420  |  neurocardiogenic syncope
C0040156  |  thyrotoxicosis
C0040038  |  thromboembolism
C0039070  |  syncope
C0038454  |  stroke
C0036454  |  visual field defects
C0033036  |  atrial extrasystole
C0027126  |  myotonic dystrophy
C0026269  |  mitral stenosis
C0018802  |  congestive heart failure
C0018801  |  heart failure
C0018799  |  heart disease
C0010068  |  coronary heart disease
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:8)
C0232197  |  fibrillation  |  7
C0039070  |  syncope  |  3
C0235480  |  paroxysmal atrial fibrillation  |  2
C0018799  |  heart disease  |  1
C0038454  |  stroke  |  1
C0018801  |  heart failure  |  1
C0039231  |  tachycardia  |  1
C1142166  |  brugada syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1805124203846516331SCN5Aumls:C0037052BeFreeMutation-specific effects of polymorphism H558R in SCN5A-related sick sinus syndrome.0.246805912010SCN5A338603929TC
rs199473556203956836331SCN5Aumls:C0037052BeFreeWe report a case of a young male with a novel SCN5A mutation (R121W) afflicted by sick sinus syndrome, progressive cardiac conduction disorder, atrial flutter and ventricular tachycardia.0.246805912010SCN5A338630342GA
rs28937319NA6331SCN5Aumls:C0037052CLINVARNA0.24680591NASCN5A338562485GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:5)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
1423404706rs10130976TArs10130976213789874.40E-07Sick sinus syndromeNANA792 Icelandic cases; 37592 Icelandic controlsIcelandic(38384)ALL(38384)EUR(38384)ALL(38384)Sick sinus syndromeHPOID:0011704Sick sinus syndromeDOID:13884sick sinus syndromeNANANANACardiovascular diseaseNAResearch Support, N.I.H., ExtramuralValidation StudiesT
1423744932rs1055061CTrs1055061213789872.20E-05Sick sinus syndromeNANA792 Icelandic cases; 37592 Icelandic controlsIcelandic(38384)ALL(38384)EUR(38384)ALL(38384)Sick sinus syndromeHPOID:0011704Sick sinus syndromeDOID:13884sick sinus syndromeNANANANACardiovascular diseaseNAResearch Support, N.I.H., ExtramuralValidation StudiesG
1423861811rs365990AGrs365990213789871.00E-08Heart rateNANA792 Icelandic cases; 37592 Icelandic controlsIcelandic(38384)ALL(38384)EUR(38384)ALL(38384)Sick sinus syndromeHPOID:0011704Sick sinus syndromeDOID:13884sick sinus syndromeNANANANACardiovascular diseaseNAResearch Support, N.I.H., ExtramuralValidation StudiesG
1423861811rs365990AGrs365990213789873.80E-05QT intervalNANA792 Icelandic cases; 37592 Icelandic controlsIcelandic(38384)ALL(38384)EUR(38384)ALL(38384)Sick sinus syndromeHPOID:0011704Sick sinus syndromeDOID:13884sick sinus syndromeNANANANACardiovascular diseaseNAResearch Support, N.I.H., ExtramuralValidation StudiesG
1423861811rs365990AGrs365990213789876.90E-04PR intervalNANA792 Icelandic cases; 37592 Icelandic controlsIcelandic(38384)ALL(38384)EUR(38384)ALL(38384)Sick sinus syndromeHPOID:0011704Sick sinus syndromeDOID:13884sick sinus syndromeNANANANACardiovascular diseaseNAResearch Support, N.I.H., ExtramuralValidation StudiesG
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:8)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0037052amsacrineD000677-sick sinus syndromeMESH:D012804marker/mechanism1877195
C0037052bupivacaineD0020452180-92-9sick sinus syndromeMESH:D012804marker/mechanism2790295
C0037052carbamazepineD002220298-46-4sick sinus syndromeMESH:D012804marker/mechanism3774685
C0037052digoxinD00407720830-75-5sick sinus syndromeMESH:D012804marker/mechanism1132120
C0037052diltiazemD00411042399-41-7sick sinus syndromeMESH:D012804marker/mechanism3134871
C0037052nimodipineD00955366085-59-4sick sinus syndromeMESH:D012804marker/mechanism11229238
C0037052propranololD011433525-66-6sick sinus syndromeMESH:D012804marker/mechanism657866
C0037052sotalolD0130153930-20-9sick sinus syndromeMESH:D012804therapeutic14593970
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)