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Details
Link-It Detail - Human Phenotype - Abnormality of humoral immunity
Debug Stats
  • ### Total Build Time: 441 ms 26.078 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 206 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=1 ms Completed: 1 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= 785 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.404 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 3.947 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=421 ms Completed: 421 ms rowSize= 18.589 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of humoral immunity HP:0005368
Parents (2)
img Abnormality of immune system physiology HP:0010978
img Abnormality of B cells HP:0002846
Children (4)
img Cryoglobulinemia HP:0100778
img Abnormality of complement system HP:0005339
img Circulating immune complexes HP:0012224
img Abnormal immunoglobulin level HP:0010701
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of immune system physiology HP:0010978
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of B cells HP:0002846
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of B cells HP:0002846
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of B cells HP:0002846
Genes (154)

Species:
human : 154
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanDEL18Q100216483Chromosome 18q deletion syndrome
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
HumanWM1100188787Macroglobulinemia, Waldenstrom, susceptibility to, 1
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanSFTPA2729238surfactant protein A2
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
HumanSFTPA1653509surfactant protein A1
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanELMOD2255520ELMO/CED-12 domain containing 2
HumanKLHDC8B200942kelch domain containing 8B
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
HumanRNF168165918ring finger protein 168, E3 ubiquitin protein ligase
img HP RolledUp, OMIM ID: 611943
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 613494
HumanERMAP114625erythroblast membrane-associated protein (Scianna blood group)
img HP RolledUp, OMIM ID: 111620
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanLMNB284823lamin B2
img HP RolledUp, OMIM ID: 608709
HumanCARD1184433caspase recruitment domain family, member 11
img HP RolledUp, OMIM ID: 606445
img HP RolledUp, OMIM ID: 615206
HumanDOCK881704dedicator of cytokinesis 8
img HP RolledUp, OMIM ID: 243700
HumanNHEJ179840nonhomologous end-joining factor 1
img HP RolledUp, OMIM ID: 611291
HumanSLEB364695systemic lupus erythematosus susceptibility 3
HumanDCLRE1C64421DNA cross-link repair 1C
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005368Abnormality of humoral immunity0self