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Details
Link-It Detail - Human Phenotype - Abnormality of coagulation
Debug Stats
  • ### Total Build Time: 38 ms 33.762 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 201 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=2 ms Completed: 2 ms rowSize= 808 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 8.606 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.121 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 20.884 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of coagulation HP:0001928
Parents (2)
img Abnormality of blood and blood-forming tissues HP:0001871
img Abnormality of metabolism/homeostasis HP:0001939
Children (26)
img Reduced von Willebrand factor activity HP:0008330
img Decreased platelet glycoprotein IIb-IIIa HP:0001975
img Reduced factor XI activity HP:0001929
img Reduced antithrombin III activity HP:0001976
img Reduced protein C activity HP:0005543
img Hypercoagulability HP:0100724
img Prolonged prothrombin time HP:0008151
img Reduced factor XII activity HP:0004841
img Chronic disseminated intravascular coagulation HP:0005520
img Abnormality of the coagulation cascade HP:0003256
img Reduced factor X activity HP:0008321
img Prolonged partial thromboplastin time HP:0003645
img Reduced prothrombin consumption HP:0003337
img Disseminated intravascular coagulation HP:0005521
img Factor X activation deficiency HP:0008354
img Abnormal bleeding HP:0001892
img Coagulopathy HP:0001925
img Prolonged bleeding time HP:0003010
img Prolonged whole-blood clotting time in severe hemophilia HP:0003229
img Reduced factor VII activity HP:0008169
img Williams factor deficiency HP:0004867
img Reduced factor XIII activity HP:0008357
img Persistent bleeding after trauma HP:0001934
img Reduced protein S activity HP:0004855
img Decreased coagulation factors IX, XI, XII HP:0005514
img Prolonged whole-blood clotting time HP:0005542
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of blood and blood-forming tissues HP:0001871
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
Genes (287)

Species:
human : 287
Page Size
Current 25
  Page 1 of 12
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
HumanIBD11100529151Inflammatory bowel disease 11
HumanOCLN100506658occludin
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanCISD2493856CDGSH iron sulfur domain 2
img HP RolledUp, OMIM ID: 604928
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP RolledUp, OMIM ID: 614077
img HP RolledUp, OMIM ID: 203300
HumanMMS338340Malignant mesothelioma, susceptibility to
img HP TAS, OMIM ID: 156240
HumanCMAL246230Capillary malformations, hereditary
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanANO6196527anoctamin 6
img HP RolledUp, OMIM ID: 262890
HumanTCPT140892thrombocytopenia, Paris-Trousseau type
img HP RolledUp, OMIM ID: 188025
HumanANIB1116833aneurysm, intracranial berry 1
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 120100
img HP RolledUp, OMIM ID: 607115
HumanCHST14113189carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
HumanRFT191869RFT1 homolog (S. cerevisiae)
img HP RolledUp, OMIM ID: 612015
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
HumanMCFD290411multiple coagulation factor deficiency 2
img HP RolledUp, OMIM ID: 613625
img HP RolledUp, OMIM ID: 227300
HumanHPS489781Hermansky-Pudlak syndrome 4
img HP RolledUp, OMIM ID: 203300
HumanMASTL84930microtubule associated serine/threonine kinase-like
HumanLCS184565lymphedema-cholestasis syndrome 1
HumanHPS384343Hermansky-Pudlak syndrome 3
img HP RolledUp, OMIM ID: 614072
img HP RolledUp, OMIM ID: 203300
HumanDTNBP184062dystrobrevin binding protein 1
img HP RolledUp, OMIM ID: 203300
img HP RolledUp, OMIM ID: 614076
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001928Abnormality of coagulation0self