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Details
Link-It Detail - Human Phenotype - Abnormality of cardiac conduction
Debug Stats
  • ### Total Build Time: 35 ms 32.779 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 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=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 4.870 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 24.562 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of cardiac conduction HP:0001665
Definition (1)
An abnormality of the electrical conduction system of the heart.
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the heart HP:0001627
Children (15)
img Prolonged QT interval HP:0001657
img Palpitations HP:0001962
img Tachycardia HP:0001649
img Ventricular arrhythmia HP:0004308
img Atrioventricular nodal disease HP:0005142
img Abnormal EKG HP:0003115
img Heart block HP:0001668
img Shortened PR interval HP:0005165
img Irregular heart beat HP:0001721
img Ventricular preexcitation HP:0004309
img Supraventricular arrhythmia HP:0005115
img Rhythm disturbances associated with pheochromocytoma HP:0001675
img EKG: T-wave abnormalities HP:0005135
img Bradycardia HP:0001662
img Cardiac arrest HP:0001695
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the heart HP:0001627
Genes (198)

Species:
human : 198
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKCNJ18100134444potassium inwardly-rectifying channel, subfamily J, member 18
img HP RolledUp, OMIM ID: 613239
HumanATFB1406216Atrial fibrillation, familial 1
img HP RolledUp, OMIM ID: 608583
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanRBM20282996RNA binding motif protein 20
img HP RolledUp, OMIM ID: 613172
HumanBRAT1221927BRCA1-associated ATM activator 1
img HP RolledUp, OMIM ID: 614498
HumanKCTD7154881potassium channel tetramerization domain containing 7
img HP ITM, OMIM ID: 611726
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
img HP RolledUp, OMIM ID: 610198
HumanMTFMT123263mitochondrial methionyl-tRNA formyltransferase
img HP RolledUp, OMIM ID: 614947
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanNEXN91624nexilin (F actin binding protein)
img HP RolledUp, OMIM ID: 613876
HumanALG1084920ALG10, alpha-1,2-glucosyltransferase
img HP RolledUp, OMIM ID: 152427
img HP RolledUp, OMIM ID: 613688
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP RolledUp, OMIM ID: 208050
HumanDCAF1780067DDB1 and CUL4 associated factor 17
img HP RolledUp, OMIM ID: 241080
HumanTMEM4379188transmembrane protein 43
img HP RolledUp, OMIM ID: 614302
img HP RolledUp, OMIM ID: 604400
HumanGATAD157798GATA zinc finger domain containing 1
img HP RolledUp, OMIM ID: 614672
HumanJPH257158junctophilin 2
img HP RolledUp, OMIM ID: 613873
HumanC10orf256652chromosome 10 open reading frame 2
img HP RolledUp, OMIM ID: 609286
HumanSCN3B55800sodium channel, voltage-gated, type III, beta subunit
img HP RolledUp, OMIM ID: 613120
HumanTMEM12755654transmembrane protein 127
img HP RolledUp, OMIM ID: 171300
HumanTRPM454795transient receptor potential cation channel, subfamily M, member 4
img HP RolledUp, OMIM ID: 604559
HumanMYOZ251778myozenin 2
img HP RolledUp, OMIM ID: 613838
HumanPRKAG251422protein kinase, AMP-activated, gamma 2 non-catalytic subunit
img HP RolledUp, OMIM ID: 600858
img HP RolledUp, OMIM ID: 194200
img HP RolledUp, OMIM ID: 261740
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanMMVP150951myxomatous mitral valve prolapse 1
img HP RolledUp, OMIM ID: 157700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001665Abnormality of cardiac conduction0self