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Details
Link-It Detail - Human Phenotype - Abnormality of the lymphatic system
Debug Stats
  • ### Total Build Time: 65 ms 26.685 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 210 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=26 ms Completed: 26 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 453 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.689 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.168 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 21.006 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the lymphatic system HP:0100763
Parents (1)
img Abnormality of the immune system HP:0002715
Children (8)
img Lymphangioma HP:0100764
img Abnormality of the spleen HP:0001743
img Abnormality of the thymus HP:0000777
img Thyroid lymphangiectasia HP:0008229
img Abnormality of the tonsils HP:0100765
img Abnormality of the lymphatic vessels HP:0100766
img Abnormality of the lymph nodes HP:0002733
img Abnormal pulmonary lymphatics HP:0006529
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the immune system HP:0002715
Genes (315)

Species:
human : 315
Page Size
Current 25
  Page 1 of 13
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOCLN100506658occludin
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanDUP22Q11.2100240738
img HP RolledUp, OMIM ID: 608363
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanNCF1653361neutrophil cytosolic factor 1
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 604131
img HP RolledUp, OMIM ID: 613985
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanCCDC39339829coiled-coil domain containing 39
img HP RolledUp, OMIM ID: 613807
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanHYLS1219844hydrolethalus syndrome 1
HumanLATD207115Laterality defects, autosomal dominant
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanADAMTS18170692ADAM metallopeptidase with thrombospondin type 1 motif, 18
img HP RolledUp, OMIM ID: 608454
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
HumanANTXR2118429anthrax toxin receptor 2
img HP RolledUp, OMIM ID: 236490
HumanCTHRC1115908collagen triple helix repeat containing 1
img HP RolledUp, OMIM ID: 614266
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100763Abnormality of the lymphatic system0self