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Details
Link-It Detail - Human Phenotype - Abnormality of the heart
Debug Stats
  • ### Total Build Time: 58 ms 30.229 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 195 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 461 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.674 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 23.381 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.019 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of the heart HP:0001627
Definition (1)
An abnormality of the `heart` (FMA:7088).
Parents (1)
img Abnormality of the cardiovascular system HP:0001626
Children (11)
img Abnormality of cardiac conduction HP:0001665
img Cardiomegaly HP:0001640
img Abnormality of the endocardium HP:0004306
img Congestive heart failure HP:0001635
img Myocardial steatosis HP:0006693
img Focal necrosis of right ventricular muscle cells HP:0003338
img Restrictive heart failure HP:0005130
img Abnormal echocardiogram HP:0003116
img Myocardial calcification HP:0006690
img Neoplasm of the heart HP:0100544
img Malformation of the heart and great vessels HP:0002564
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the cardiovascular system HP:0001626
Genes (830)

Species:
human : 830
Page Size
Current 25
  Page 1 of 34
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
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
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
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
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
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
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanPRBNS100301572Pierre Robin syndrome
img HP RolledUp, OMIM ID: 261800
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP RolledUp, OMIM ID: 612626
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001627Abnormality of the heart0self