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Details
Link-It Detail - Human Phenotype - Abnormalities of the peripheral arteries
Debug Stats
  • ### Total Build Time: 72 ms 27.032 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 215 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= 792 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 1.080 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 3.035 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 20.755 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)
Abnormalities of the peripheral arteries HP:0005114
Parents (2)
img Systemic artery abnormality HP:0002620
img Abnormality of the systemic arterial tree HP:0011004
Children (3)
img Abnormality of the celiac artery HP:0012326
img Arterial stenosis HP:0100545
img Peripheral arterial disease HP:0004950
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Systemic artery abnormality HP:0002620
img All HP:0000001img Phenotypic abnormality HP:00001186img Systemic artery abnormality HP:0002620
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the systemic arterial tree HP:0011004
Genes (100)

Species:
human : 100
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
img HP RolledUp, OMIM ID: 610655
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP RolledUp, OMIM ID: 208050
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP RolledUp, OMIM ID: 611775
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
HumanXYLT264132xylosyltransferase II
HumanXYLT164131xylosyltransferase I
HumanTMEM12755654transmembrane protein 127
img HP RolledUp, OMIM ID: 171300
HumanDHTKD155526dehydrogenase E1 and transketolase domain containing 1
img HP RolledUp, OMIM ID: 614025
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img HP RolledUp, OMIM ID: 242900
HumanKIF1B23095kinesin family member 1B
img HP RolledUp, OMIM ID: 171300
HumanTREX111277three prime repair exonuclease 1
img HP RolledUp, OMIM ID: 192315
HumanPPP1R1710842protein phosphatase 1, regulatory subunit 17
HumanDHS10774dehydrated hereditary stomatocytosis
img HP RolledUp, OMIM ID: 177720
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
img HP RolledUp, OMIM ID: 249270
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 176670
HumanSH2B310019SH2B adaptor protein 3
img HP RolledUp, OMIM ID: 133100
HumanGTF2IRD19569GTF2I repeat domain containing 1
img HP RolledUp, OMIM ID: 194050
HumanSNAP299342synaptosomal-associated protein, 29kDa
img HP RolledUp, OMIM ID: 609528
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP RolledUp, OMIM ID: 308300
HumanWRN7486Werner syndrome, RecQ helicase-like
img HP RolledUp, OMIM ID: 277700
HumanBEST17439bestrophin 1
img HP RolledUp, OMIM ID: 193220
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005114Abnormalities of the peripheral arteries0self