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Details
Link-It Detail - Disease - Blood Group Incompatibility
Debug Stats
  • ### Total Build Time: 20 ms 29.982 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 352 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 497 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 996 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 997 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.793 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 10.077 KB
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 12.965 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Blood Group Incompatibility C0005806
Definition (1)
An antigenic mismatch between donor and recipient blood. Antibodies present in the recipient's serum may be directed against antigens in the donor product. Such a mismatch may result in a transfusion reaction in which, for example, donor blood is hemolyzed. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Hematologic Diseases C0018939
img Immune System Diseases C0021053
Children (2)
img Erythroblastosis, Fetal C0014761
img Rh Isoimmunization C0035404
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189393img Hematologic Diseases C0018939
img Immune System Diseases C0021053img Hematologic Diseases C00189392img Immune System Diseases C0021053
Relationships (25)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 9
diso_​to_​diso : 6
diso_​to_​phys : 2


Relationships:
none : 24
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT222img ABO Blood-Group System C0000778
DISO_to_ANAT199img ABO Blood-Group System C0000778
DISO_to_CHEM53img Isoantibodies C0022144
DISO_to_ANAT51img In Blood C0005768
DISO_to_DISO43img Complication Aspects C1171258
DISO_to_CHEM38img Alloantibodies C0022144
DISO_to_DISO36img Complication Aspects C1171258
DISO_to_PHYS30img Graft Rejection C0018129
DISO_to_CHEM27img Blood Group Antigens C0005804
DISO_to_ANAT25img In Blood C0005768
DISO_to_ANAT25img Rh-Hr Blood-Group System C0035406
DISO_to_ANAT22img Rh-Hr Blood-Group System C0035406
DISO_to_PHYS22img Graft Rejection C0018129
DISO_to_ANAT20img Erythrocytes C0014792
DISO_to_DISO20img Hemolysis C0019054
DISO_to_CHEM16img Antibodies, Monoclonal C0003250
DISO_to_DISO16img Hemolysis C0019054
DISO_to_CHEM15img Antibodies, Monoclonal C0003250
DISO_to_CHEM15img Immunosuppressive Agents C0021081
DISO_to_CHEM14img Antibodies C0003241
DISO_to_ANAT13img Erythrocytes C0014792
DISO_to_CHEM13img Blood Group Antigens C0005804
DISO_to_CHEM13img Immunosuppressive Agents C0021081
DISO_to_DISO13img Erythroblastosis, Fetal C0014761
DISO_to_DISOpermuted_term_ofimg Blood Group Incompatibilities C0005806
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanTALDO16888transaldolase 1
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanPTH1R5745parathyroid hormone 1 receptor
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanPKLR5313pyruvate kinase, liver and RBC
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanNEU14758sialidase 1 (lysosomal sialidase)
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanHADHB3032hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanHADHA3030hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanGUSB2990glucuronidase, beta
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanGLE12733GLE1 RNA export mediator
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanGBE12632glucan (1,4-alpha-), branching enzyme 1
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanGBA2629glucosidase, beta, acid
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanFLT42324fms-related tyrosine kinase 4
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanERBB32065v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 3
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanSLC26A21836solute carrier family 26 (anion exchanger), member 2
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanCOL2A11280collagen, type II, alpha 1
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
INFERRED, Score=800, UMLKSK CUI: C0005806
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
INFERRED, Score=800, UMLKSK CUI: C0005806
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0005806Blood Group Incompatibility0self