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Details
Link-It Detail - Human Phenotype - Abnormality of the left ventricular outflow tract
Debug Stats
  • ### Total Build Time: 39 ms 14.706 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 224 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 225 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 454 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 450 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 1.169 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 11.028 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.043 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the left ventricular outflow tract HP:0011103
Definition (1)
An abnormality of the `outflow tract of the left ventricle` (FMA:9473).
Parents (1)
img Abnormality of the left ventricle HP:0001711
Children (1)
img Subvalvular aortic stenosis HP:0001682
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the left ventricle HP:0001711
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanMYLK285366myosin light chain kinase 2
img HP RolledUp, OMIM ID: 192600
HumanTAB223118TGF-beta activated kinase 1/MAP3K7 binding protein 2
img HP RolledUp, OMIM ID: 614980
HumanHDAC49759histone deacetylase 4
img HP RolledUp, OMIM ID: 600430
HumanCEP579702centrosomal protein 57kDa
img HP RolledUp, OMIM ID: 614114
HumanTNNC17134troponin C type 1 (slow)
img HP RolledUp, OMIM ID: 192600
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
img HP RolledUp, OMIM ID: 151100
HumanMYH74625myosin, heavy chain 7, cardiac muscle, beta
img HP RolledUp, OMIM ID: 192600
HumanMYH64624myosin, heavy chain 6, cardiac muscle, alpha
img HP RolledUp, OMIM ID: 192600
HumanFRDA22420Friedreich ataxia 2
HumanNKX2-51482
img HP RolledUp, OMIM ID: 108900
HumanCAV3859caveolin 3
img HP RolledUp, OMIM ID: 192600
HumanBDMR626brachydactyly-mental retardation syndrome
img HP RolledUp, OMIM ID: 600430
HumanSLC25A4291solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
img HP RolledUp, OMIM ID: 192600
HumanACTC170actin, alpha, cardiac muscle 1
img HP RolledUp, OMIM ID: 192600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011103Abnormality of the left ventricular outflow tract0self