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Details
Link-It Detail - Human Phenotype - Abnormality of the lymph nodes
Debug Stats
  • ### Total Build Time: 31 ms 30.536 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 205 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 192 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=3 ms Completed: 3 ms rowSize= 791 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.361 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.104 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 23.741 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the lymph nodes HP:0002733
Definition (1)
A `lymph node` (FMA:5034) abnormality.
Parents (2)
img Abnormality of the immune system HP:0002715
img Abnormality of the lymphatic system HP:0100763
Children (7)
img Abnormal lymph node histology HP:0008149
img Follicular hyperplasia HP:0002729
img Lymphadenitis HP:0002840
img Lymphadenopathy HP:0002716
img Chronic noninfectious lymphadenopathy HP:0002730
img Lymph node hypoplasia HP:0002732
img Absence of lymph node germinal center HP:0002849
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the immune system HP:0002715
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the lymphatic system HP:0100763
Genes (87)

Species:
human : 87
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanCTHRC1115908collagen triple helix repeat containing 1
img HP RolledUp, OMIM ID: 614266
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 240500
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 607115
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP RolledUp, OMIM ID: 611775
HumanRHBDF279651rhomboid 5 homolog 2 (Drosophila)
img HP RolledUp, OMIM ID: 148500
HumanPORCN64840porcupine homolog (Drosophila)
img HP RolledUp, OMIM ID: 305600
HumanDCLRE1C64421DNA cross-link repair 1C
img HP RolledUp, OMIM ID: 603554
img HP RolledUp, OMIM ID: 602450
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
img HP RolledUp, OMIM ID: 186580
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanAICDA57379activation-induced cytidine deaminase
img HP RolledUp, OMIM ID: 605258
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
HumanSLC29A355315solute carrier family 29 (equilibrative nucleoside transporter), member 3
img HP RolledUp, OMIM ID: 602782
HumanWWOX51741WW domain containing oxidoreductase
img HP RolledUp, OMIM ID: 133239
HumanASCC151008activating signal cointegrator 1 complex subunit 1
img HP RolledUp, OMIM ID: 614266
HumanFOXP350943forkhead box P3
img HP RolledUp, OMIM ID: 304790
HumanDEC150514deleted in esophageal cancer 1
img HP RolledUp, OMIM ID: 133239
HumanICOS29851inducible T-cell co-stimulator
img HP RolledUp, OMIM ID: 607594
img HP RolledUp, OMIM ID: 240500
HumanHPLH127259hemophagocytic lymphohistiocytosis 1
img HP RolledUp, OMIM ID: 267700
HumanLEMD323592LEM domain containing 3
img HP RolledUp, OMIM ID: 166700
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
img HP RolledUp, OMIM ID: 240500
HumanVPS13A23230vacuolar protein sorting 13 homolog A (S. cerevisiae)
img HP RolledUp, OMIM ID: 200150
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002733Abnormality of the lymph nodes0self