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Details
Link-It Detail - Disease - SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
Debug Stats
  • ### Total Build Time: 20 ms 10.182 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 6.969 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 1.594 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE C1837845
Relationships (16)

Relation Types:
diso_​to_​diso : 16


Relationships:
alias_​of : 1
manifestation_​of : 15
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Absent P waves C1837847
DISO_to_DISOmanifestation_ofimg Allelic disorder is Brugada syndrome (601144) C1837855
DISO_to_DISOmanifestation_ofimg Allelic disorder is long QT syndrome-3 (LQT3, 603830) C1837854
DISO_to_DISOmanifestation_ofimg Atrial inexcitability C1837846
DISO_to_DISOmanifestation_ofimg Caused by mutation in the sodium channel, voltage-gated, type V, alpha polypeptide gene (SCN5A, 600163.0025) C1837852
DISO_to_DISOmanifestation_ofimg Heterozygous mutation carriers may show first-degree heart block or conduction delay C1837851
DISO_to_DISOmanifestation_ofimg Increased His-ventricular conduction time C1837849
DISO_to_DISOmanifestation_ofimg Irregular heart beat C0237314
DISO_to_DISOmanifestation_ofimg No structural defects C1837850
DISO_to_DISOmanifestation_ofimg Onset in utero, infancy, or early childhood C1837853
DISO_to_DISOmanifestation_ofimg Prolonged QRS duration C1837848
DISO_to_DISOalias_ofimg SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE C1837845
DISO_to_DISOmanifestation_ofimg See also autosomal dominant sick sinus syndrome (163800) C1837856
DISO_to_DISOmanifestation_ofimg Sinus arrest C0178428
DISO_to_DISOmanifestation_ofimg Sinus bradycardia C0085610
DISO_to_DISOmanifestation_ofimg Ventricular escape rhythm C0232216
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCN5A6331sodium channel, voltage-gated, type V, alpha subunit
img GAD, Score=1000, Pubmed Id: 14523039, UMLKSK CUI: C1837845
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1837845SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE0self