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Details
Link-It Detail - Human Phenotype - Abnormality of the cardiovascular system
Debug Stats
  • ### Total Build Time: 84 ms 28.546 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 215 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 241 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=0 Completed: 0 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 2.675 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.158 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=75 ms Completed: 75 ms rowSize= 22.656 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.034 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cardiovascular system HP:0001626
Definition (1)
The cardiovascular system consists of the heart, vasculature, and the lymphatic system.
Parents (1)
img Phenotypic abnormality HP:0000118
Children (8)
img Abnormality of the heart HP:0001627
img Syncope HP:0001279
img Abnormality of the vasculature HP:0002597
img Hypertension HP:0000822
img Atherosclerosis HP:0002621
img Abnormality of cardiovascular system physiology HP:0011025
img Hypotension HP:0002615
img Abnormality of the fetal cardiovascular system HP:0010948
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (1214)

Species:
human : 1214
Page Size
Current 25
  Page 1 of 49
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanCMH21100909387Cardiomyopathy, familial hypertrophic, 21
img HP RolledUp, OMIM ID: 614676
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanGFND1100689213Glomerulopathy with fibronectin deposits 1
img HP RolledUp, OMIM ID: 137950
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanIGAN2100653384IgA nephropathy, susceptibility to, 2
img HP RolledUp, OMIM ID: 613944
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL7Q11.23100653380
img HP RolledUp, OMIM ID: 613729
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanCPVT3100653371Ventricular tachycardia, catecholaminergic polymorphic, 3
img HP RolledUp, OMIM ID: 614021
HumanIBD11100529151Inflammatory bowel disease 11
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanOCLN100506658occludin
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanATPLS100499532antiphospholipid syndrome, familial
img HP RolledUp, OMIM ID: 107320
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001626Abnormality of the cardiovascular system0self