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Details
Link-It Detail - Human Phenotype - Abnormality of the cardiac septa
Debug Stats
  • ### Total Build Time: 41 ms 28.951 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 207 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
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  • 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=5 ms Completed: 5 ms rowSize= 2.729 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.179 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=24 ms Completed: 24 ms rowSize= 23.218 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cardiac septa HP:0001671
Parents (1)
img Malformation of the heart and great vessels HP:0002564
Children (8)
img Abnormality of the ventricular septum HP:0010438
img Abnormality of the atrial septum HP:0011994
img Endocardial fibroelastosis HP:0001706
img Complete atrioventricular canal defect HP:0001674
img Asymmetric septal hypertrophy HP:0001670
img Abnormality of the atrial septum HP:0001630
img Atrioventricular canal defect HP:0006695
img Congenital septal defect HP:0004760
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Malformation of the heart and great vessels HP:0002564
Genes (276)

Species:
human : 276
Page Size
Current 25
  Page 1 of 12
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL7Q11.23100653380
img HP RolledUp, OMIM ID: 613729
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP IEA, OMIM ID: 612626
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDUP22Q11.2100240738
img HP RolledUp, OMIM ID: 608363
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP TAS, OMIM ID: 612474
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanAUTS14100187724autism, susceptibility to, 14
img HP RolledUp, OMIM ID: 611913
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001671Abnormality of the cardiac septa0self