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Details
Link-It Detail - Disease - Eosinophilia
Debug Stats
  • ### Total Build Time: 75 ms 46.410 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 219 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=10 ms Completed: 10 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.868 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.515 KB
  • CONCEPT_RELATIONSHIPS gt=44 ms Completed: 44 ms rowSize= 13.556 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 27.044 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Eosinophilia C0014457
Definition (1)
Abnormal increase of EOSINOPHILS in the blood, tissues or organs.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Leukocyte Disorders C0023510
Children (4)
img Eosinophilia-Myalgia Syndrome C0085179
img Eosinophilic Granuloma C0014461
img Angiolymphoid Hyperplasia with Eosinophilia C0002989
img Hypereosinophilic Syndrome C1540912
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Leukocyte Disorders C0023510
Relationships (148)

Relation Types:
diso_​to_​anat : 16
diso_​to_​chem : 27
diso_​to_​diso : 103
diso_​to_​phen : 2


Relationships:
none : 129
associated_​with : 1
classifies : 1
expanded_​form_​of : 1
mapped_​to : 15
use : 1
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO371img Complication Aspects C1171258
DISO_to_DISO267img Complication Aspects C1171258
DISO_to_DISO250img Esophagitis C0014868
DISO_to_DISO160img chemically induced C0007994
DISO_to_DISO124img Esophagitis C0014868
DISO_to_ANAT116img Eosinophils C0014467
DISO_to_DISO89img Asthma C0004096
DISO_to_DISO88img chemically induced C0007994
DISO_to_DISO87img Asthma C0004096
DISO_to_ANAT79img In Blood C0005768
DISO_to_DISO75img Gastroenteritis C0017160
DISO_to_DISO70img 0-71 DRUG ERUPTIONS C0011609
DISO_to_ANAT68img In Blood C0005768
DISO_to_DISO63img Fasciitis C0015645
DISO_to_DISO60img Fasciitis C0015645
DISO_to_ANAT54img Eosinophils C0014467
DISO_to_PHEN54img genetic aspects C0017399
DISO_to_DISO53img Gastroenteritis C0017160
DISO_to_DISO42img Drug Allergy C0013182
DISO_to_PHEN42img genetic aspects C0017399
DISO_to_DISO39img Enteritis C0014335
DISO_to_DISO38img FOLLICULITIS C0016436
DISO_to_DISO37img Cellulitis C0007642
DISO_to_CHEM33img Interleukin-5 C0021759
DISO_to_DISO33img Gastrointestinal Diseases C0017178
Genes (29)

Species:
human : 29
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFIP1L181608factor interacting with PAPOLA and CPSF1
img GENERIF, Score=861, Pubmed Id: 15284118, UMLKSK CUI: C0014457
HumanIL2564806interleukin 25
img GENERIF, Score=1000, Pubmed Id: 12239140, UMLKSK CUI: C0014457
HumanDCLRE1C64421DNA cross-link repair 1C
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanCHIC226511cysteine-rich hydrophobic domain 2
img GENERIF, Score=1000, Pubmed Id: 12842979, UMLKSK CUI: C0014457
HumanTNFRSF10C8794tumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain
img GENERIF, Score=812, Pubmed Id: 17265502, UMLKSK CUI: C0014457
HumanTP638626tumor protein p63
img GENERIF, Score=812, Pubmed Id: 15001991, UMLKSK CUI: C0014457
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanSTAT66778signal transducer and activator of transcription 6, interleukin-4 induced
img GAD, Score=1000, Pubmed Id: 11912176, UMLKSK CUI: C0014457
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanCCL176361chemokine (C-C motif) ligand 17
img GENERIF, Score=1000, Pubmed Id: 18395252, UMLKSK CUI: C0014457
HumanRNASE36037ribonuclease, RNase A family, 3
INFERRED, Score=800, UMLKSK CUI: C0014457
HumanRAG25897recombination activating gene 2
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanRAG15896recombination activating gene 1
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanPTGDS5730prostaglandin D2 synthase 21kDa (brain)
img GENERIF, Score=861, Pubmed Id: 11751991, UMLKSK CUI: C0014457
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
img OMIM, Score=833, UMLKSK CUI: C0014457
HumanIL103586interleukin 10
img GAD, Score=1000, Pubmed Id: 11668616, UMLKSK CUI: C0014457
HumanIL53567interleukin 5 (colony-stimulating factor, eosinophil)
img GENERIF, Score=827, Pubmed Id: 17581195, UMLKSK CUI: C0014457
img GENERIF, Score=1000, Pubmed Id: 18395252, UMLKSK CUI: C0014457
img GAD, Score=1000, Pubmed Id: 9758611, UMLKSK CUI: C0014457
HumanIL2RA3559interleukin 2 receptor, alpha
img GENERIF, Score=1000, Pubmed Id: 12486319, UMLKSK CUI: C0014457
HumanGFI12672growth factor independent 1 transcription repressor
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanETV62120ets variant 6
img GENERIF, Score=1000, Pubmed Id: 12505259, UMLKSK CUI: C0014457
HumanELANE1991elastase, neutrophil expressed
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanCCNT1904cyclin T1
INFERRED, Score=800, UMLKSK CUI: C0014457
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img OMIM, Score=1000, UMLKSK CUI: C0014457
HumanCAPN3825calpain 3, (p94)
img OMIM, Score=833, UMLKSK CUI: C0014457
HumanFAS355Fas cell surface death receptor
img OMIM, Score=1000, UMLKSK CUI: C0014457
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0014457Eosinophilia0self