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Details
Link-It Detail - Human Phenotype - Abnormality of the left ventricle
Debug Stats
  • ### Total Build Time: 29 ms 27.014 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 208 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=2 ms Completed: 2 ms rowSize= 453 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.438 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.168 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 22.591 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the left ventricle HP:0001711
Parents (1)
img Abnormality of cardiac ventricle HP:0001713
Children (4)
img Impaired left ventricular function HP:0005162
img Left ventricular hypertrophy HP:0001712
img Double outlet left ventricle HP:0011581
img Abnormality of the left ventricular outflow tract HP:0011103
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of cardiac ventricle HP:0001713
Genes (57)

Species:
human : 57
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCMH21100909387Cardiomyopathy, familial hypertrophic, 21
img HP RolledUp, OMIM ID: 614676
HumanMYMY4100653379Moyamoya disease 4
img HP IEA, OMIM ID: 300845
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanBBS5129880Bardet-Biedl syndrome 5
img HP RolledUp, OMIM ID: 209900
HumanTTC8123016tetratricopeptide repeat domain 8
img HP RolledUp, OMIM ID: 209900
HumanNEXN91624nexilin (F actin binding protein)
img HP RolledUp, OMIM ID: 613876
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 209900
HumanMYLK285366myosin light chain kinase 2
HumanARL684100ADP-ribosylation factor-like 6
img HP RolledUp, OMIM ID: 209900
HumanCEP29080184centrosomal protein 290kDa
img HP RolledUp, OMIM ID: 209900
HumanBBS1079738Bardet-Biedl syndrome 10
img HP RolledUp, OMIM ID: 209900
HumanFKRP79147fukutin related protein
img HP RolledUp, OMIM ID: 613153
img HP RolledUp, OMIM ID: 606612
img HP RolledUp, OMIM ID: 607155
HumanCCDC28B79140coiled-coil domain containing 28B
img HP RolledUp, OMIM ID: 209900
HumanEPG557724ectopic P-granules autophagy protein 5 homolog (C. elegans)
img HP RolledUp, OMIM ID: 242840
HumanJPH257158junctophilin 2
img HP RolledUp, OMIM ID: 613873
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
img HP RolledUp, OMIM ID: 614654
HumanBBS755212Bardet-Biedl syndrome 7
img HP RolledUp, OMIM ID: 209900
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 209900
HumanMYOZ251778myozenin 2
img HP RolledUp, OMIM ID: 613838
HumanWDPCP51057WD repeat containing planar cell polarity effector
img HP RolledUp, OMIM ID: 209900
HumanPOMT229954protein-O-mannosyltransferase 2
img HP RolledUp, OMIM ID: 613156
HumanBBS927241Bardet-Biedl syndrome 9
img HP RolledUp, OMIM ID: 209900
HumanTPK127010thiamin pyrophosphokinase 1
img HP RolledUp, OMIM ID: 614458
HumanB3GAT326229beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)
img HP RolledUp, OMIM ID: 245600
HumanTAB223118TGF-beta activated kinase 1/MAP3K7 binding protein 2
img HP RolledUp, OMIM ID: 614980
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001711Abnormality of the left ventricle0self