Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

Total absence von Willebrand factor multimers

ID: HP:0030134

Type: http://bio2vec.net/ontology/phenotype

Label: Total absence von Willebrand factor multimers

Synonyms: Total absence von Willebrand factor multimers

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Total absence von Willebrand factor multimers

HP:0030134
Abnormal von Willebrand factor multimer distribution

HP:0030131
Absence of intermediate von Willibrand factor multimers

HP:0030135
Absence of large von Willibrand factor multimers

HP:0030132
Impaired von Willibrand factor collagen binding activity

HP:0030130
Enhanced ristocetin cofactor assay activity

HP:0030136
Abnormal presence of ultra-large von Willebrand factor multimers

HP:0030133
Decrease in high molecular weight von Willebrand factor Multimers

HP:0040225
Reduced von Willebrand factor activity

HP:0008330
Decreased level of plasminogen

HP:0040228
Impaired binding of factor VIII to VWF

HP:0040237
Abnormality of von Willebrand factor

HP:0012146
Elevated factor V activity

HP:0011996
Impaired ristocetin-induced platelet aggregation

HP:0011871
Reduced quantity of Von Willebrand factor

HP:0012147
Decreased level of histidine-rich glycoprotein

HP:0040227
Increased plasma vitamin K epoxide after vitamin K supplementation

HP:0040239
Impaired ristocetin cofactor assay activity

HP:0030129
Factor XIII subunit B deficiency

HP:0040234
Decreased level of tissue plasminogen activator

HP:0040230
Reduced prothrombin consumption

HP:0003337
Decreased level of thrombomodulin

HP:0040229
Factor X activation deficiency

HP:0008354
Decreased level of heparin co-factor II

HP:0040226
Reduced factor VIII activity

HP:0003125
Hypofibrinogenemia

HP:0011900
Factor XIII subunit A deficiency

HP:0040233
Reduced factor XIII activity

HP:0008357
Hyperfibrinolysis

HP:0040236
Increased ratio of VWF propeptide to VWF antigen

HP:0040240
Prolonged Russell'\''s viper venom time

HP:0040244
Hyperfibrinogenemia

HP:0011899
Abnormality of fibrinolysis

HP:0040224
Dysfibrinogenemia

HP:0011901
Impaired arachidonic acid-induced platelet aggregation

HP:0011870
Abnormality of circulating fibrinogen

HP:0011898
Reduced factor IX activity

HP:0011858
Reduced alpha-2-antiplasmin activity

HP:0040245
Reduced euglobulin clot lysis time

HP:0040247
Reduced antithrombin antigen

HP:0040246
small protein activating enzyme binding

GO:0044388
Resistance to activated protein C

HP:0012175
Delayed onset bleeding

HP:0040232
Reduced antithrombin III activity

HP:0001976
regulation of B cell antigen processing and presentation

GO:0002622
Reduced plasminogen activator inhibitor 1 antigen

HP:0040249
Reduced factor XII activity

HP:0004841
Infantile axial hypotonia

HP:0009062
Post-transfusion thrombocytopenia

HP:0004813
Grade II preterm intraventricular hemorrhage

HP:0030749
Abnormal onset of bleeding

HP:0040231
positive regulation of protein localization to cell cortex

GO:1904778
Macrothrombocytopenia

HP:0040185
Folate-unresponsive megaloblastic anemia

HP:0004826
obsolete cellular response to Dizocilpine

GO:1905107
regulation of protein localization to cell cortex

GO:1904776
Reduced factor V activity

HP:0003225
Impaired thrombin-induced platelet aggregation

HP:0011872
regulation of protein kinase D signaling

GO:1903570
Grade I preterm intraventricular hemorrhage

HP:0030748
Refractory anemia with ringed sideroblasts

HP:0004828
Reduced prothrombin antigen

HP:0040250
Priapism

HP:0200023
Cystic artery pseudoaneurysm

HP:0030170
Elevated hemoglobin A1c

HP:0040217
Prolonged whole-blood clotting time

HP:0005542
Single lineage myelodysplasia

HP:0012150
regulation of CD4-positive

GO:0032829
Prolonged euglobulin clot lysis time

HP:0040243
peripheral nervous system axon regeneration

GO:0014012
Hypoplastic pilosebaceous units

HP:0007515
Gerbode ventricular septal defect

HP:0011621
Reduced plasminogen activator inhibitor 1 activity

HP:0040248
no_name

GO:0043340
Gallbladder perforation

HP:0030154
Bifid penis

HP:0100599
HbS hemoglobin

HP:0045047
Encephalomalacia

HP:0040197
Reduced protein C activity

HP:0005543
Cortical diaphyseal irregularity of the upper limbs

HP:0003858
Reduced factor XI activity

HP:0001929
Decreased mean platelet volume

HP:0005537
no_name

GO:0030607
regulation of T cell antigen processing and presentation

GO:0002625
Postprandial hyperlactemia

HP:0011997
Reduced natural killer cell number

HP:0040218
Intermittent thrombocytopenia

HP:0004854
regulation of interleukin-22 biosynthetic process

GO:0045393
mesonephric interstitial fibroblast fate commitment

GO:0061268
Partial development of the penile shaft

HP:0008708
ovarian dermoid cyst with angiosarcoma

DOID:6632
Reduced kininogen activity

HP:0005527
signal transduction involved in mitotic spindle assembly checkpoint

GO:0072480
Methylmalonic acidemia

HP:0002912
Abnormality of corpus cavernosum

HP:0100623
Abnormality of the kinin-kallikrein system

HP:0005559
Increased HbA2 hemoglobin

HP:0045048
indole-3-glycerol-phosphate lyase activity

GO:0033984
phosphoribokinase activity

GO:0050195
Prolonged bleeding after dental extraction

HP:0006298

Neighbourhood Visualization