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Details
Link-It Detail - Human Phenotype - Abnormality of the heart valves
Debug Stats
  • ### Total Build Time: 98 ms 27.787 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 206 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=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= 464 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.769 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.179 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=87 ms Completed: 87 ms rowSize= 23.016 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the heart valves HP:0001654
Parents (1)
img Malformation of the heart and great vessels HP:0002564
Children (5)
img Cardiac valve calcification HP:0005146
img Abnormality of the atrioventricular valves HP:0006705
img Abnormality of the aortic valve HP:0001646
img Abnormality of the pulmonary valve HP:0001641
img Increased prevalence of valvular disease HP:0001726
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Malformation of the heart and great vessels HP:0002564
Genes (184)

Species:
human : 184
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanAUTS14100187724autism, susceptibility to, 14
img HP RolledUp, OMIM ID: 611913
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanMMVP3100034705Mitral valve prolapse, myxomatous 3
img HP RolledUp, OMIM ID: 610840
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
img HP RolledUp, OMIM ID: 600721
HumanKIF7374654kinesin family member 7
img HP RolledUp, OMIM ID: 200990
HumanMMVP2352956myxomatous mitral valve prolapse 2
img HP RolledUp, OMIM ID: 607829
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img HP RolledUp, OMIM ID: 269000
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanEVC2132884Ellis van Creveld syndrome 2
img HP TAS, OMIM ID: 225500
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001654Abnormality of the heart valves0self