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Details
Link-It Detail - Disease - Leukocyte Disorders
Debug Stats
  • ### Total Build Time: 161 ms 37.985 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 263 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 3.097 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=88 ms Completed: 88 ms rowSize= 12.769 KB
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 18.112 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Leukocyte Disorders C0023510
Definition (1)
Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hematologic Diseases C0018939
Children (7)
img Leukopenia C0023530
img Leukostasis C0282548
img Eosinophilia C0014457
img Pelger-Huet Anomaly C0030779
img Phagocyte Bactericidal Dysfunction C0031306
img Infectious Mononucleosis C0021345
img Leukocytosis C0023518
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189393img Hematologic Diseases C0018939
Relationships (42)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 38
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 4
classified_​as : 4
isa : 14
mapped_​to : 20
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT8img Neutrophils C0027950
DISO_to_DISO7img Complication Aspects C1171258
DISO_to_ANAT5img Neutrophils C0027950
DISO_to_DISO3img Complication Aspects C1171258
DISO_to_DISOmapped_toimg 640-645 ABNORMAL WHITE BLOOD CELLS C0152009
DISO_to_DISOmapped_toimg Abnormal granulocyte destruction C0302094
DISO_to_DISOmapped_toimg Abnormal granulocyte production C0221144
DISO_to_DISOmapped_toimg Abnormal lymphocyte destruction C0302102
DISO_to_DISOmapped_toimg Abnormal lymphocyte production C0302098
DISO_to_DISOmapped_toimg Abnormal monocytes C0580319
DISO_to_DISOmapped_toimg Atypical lymphocyte observed C0427546
DISO_to_DISOmapped_toimg Benign white cell disorder C0398572
DISO_to_DISOmapped_toimg C-40 WHITE BLOOD CELL DISORDERS: GENERAL TERMS C0023510
DISO_to_DISOmapped_toimg C-41 DISORDERS OF NEUTROPHILS C0272157
DISO_to_DISOisaimg C-418 QUALITATIVE ABNORMALITIES OF GRANULOCYTES C0272183
DISO_to_DISOclassified_asimg Congenital Leucocyte Abnormality C0017377
DISO_to_DISOmapped_toimg Decreased lymphocyte production C0302100
DISO_to_DISOisaimg Disorder involving basophils and mast cells C1285260
DISO_to_DISOmapped_toimg Disorder of basophils C1563248
DISO_to_DISOisaimg Disorder of eosinophil C1691020
DISO_to_DISOclassified_asimg Eosinophilia C0014457
DISO_to_DISOmapped_toimg Eosinophilic disorder C1306759
DISO_to_DISOclassified_asimg Function dis neutrophils C0016808
DISO_to_DISOisaimg GRANULOCYTOSIS C1282609
DISO_to_DISOisaimg Granulation anomaly C1260900
Genes (120)

Species:
human : 120
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanFIP1L181608factor interacting with PAPOLA and CPSF1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanIL2564806interleukin 25
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSLEB364695systemic lupus erythematosus susceptibility 3
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanDCLRE1C64421DNA cross-link repair 1C
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSALL457167sal-like 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanBANK155024B-cell scaffold protein with ankyrin repeats 1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSLCO1B328234solute carrier organic anion transporter family, member 1B3
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanCHIC226511cysteine-rich hydrophobic domain 2
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanMASP210747mannan-binding lectin serine peptidase 2
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanSLC35A110559solute carrier family 35 (CMP-sialic acid transporter), member A1
INFERRED, Score=800, UMLKSK CUI: C0023510
HumanRECQL49401RecQ protein-like 4
INFERRED, Score=800, UMLKSK CUI: C0023510
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023510Leukocyte Disorders0self