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Details
Link-It Detail - Human Phenotype - Abnormal leukocyte count
Debug Stats
  • ### Total Build Time: 41 ms 24.666 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 216 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=3 ms Completed: 3 ms rowSize= 446 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 748 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.088 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 19.844 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal leukocyte count HP:0011893
Definition (1)
Number of leukocytes per volume of blood beyond normal limits.
Parents (1)
img Abnormality of leukocytes HP:0001881
Children (2)
img Leukopenia HP:0001882
img Leukocytosis HP:0001974
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of leukocytes HP:0001881
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of leukocytes HP:0001881
Genes (111)

Species:
human : 111
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img HP RolledUp, OMIM ID: 152700
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
img HP RolledUp, OMIM ID: 152700
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
img HP RolledUp, OMIM ID: 152700
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 120100
img HP RolledUp, OMIM ID: 607115
img HP RolledUp, OMIM ID: 191900
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanG6PC392579glucose 6 phosphatase, catalytic, 3
img HP RolledUp, OMIM ID: 612541
HumanFERMT383706fermitin family member 3
img HP RolledUp, OMIM ID: 612840
HumanDOCK881704dedicator of cytokinesis 8
img HP RolledUp, OMIM ID: 243700
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP RolledUp, OMIM ID: 611775
HumanPALB279728partner and localizer of BRCA2
img HP RolledUp, OMIM ID: 610832
HumanSLEB364695systemic lupus erythematosus susceptibility 3
img HP RolledUp, OMIM ID: 152700
HumanDCLRE1C64421DNA cross-link repair 1C
img HP RolledUp, OMIM ID: 603554
HumanNOD264127nucleotide-binding oligomerization domain containing 2
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanSALL457167sal-like 4 (Drosophila)
img HP RolledUp, OMIM ID: 147750
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
HumanADCK356997aarF domain containing kinase 3
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
HumanLMBRD155788LMBR1 domain containing 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011893Abnormal leukocyte count0self