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.

Impaired thrombin-induced platelet aggregation

ID: HP:0011872

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

Label: Impaired thrombin-induced platelet aggregation

Synonyms: Impaired thrombin-induced platelet aggregation

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Impaired thrombin-induced platelet aggregation

HP:0011872
Spontaneous platelet aggregation

HP:0030403
Impaired ristocetin-induced platelet aggregation

HP:0011871
Impaired thromboxane A2 agonist-induced platelet aggregation

HP:0011894
Decreased platelet glycoprotein VI

HP:0011881
Decreased platelet glycoprotein Ib-IX-V

HP:0011879
Decreased platelet P2Y12 receptor

HP:0011882
Abnormal platelet membrane protein expression

HP:0011878
Impaired arachidonic acid-induced platelet aggregation

HP:0011870
Abnormal platelet granule secretion

HP:0030396
Impaired collagen-induced platelet aggregation

HP:0008320
Abnormal platelet lysosome secretion

HP:0030400
Impaired epinephrine-induced platelet aggregation

HP:0008148
Impaired platelet aggregation

HP:0003540
Increased RIPA

HP:0040241
Abnormal platelet alpha granule secretion

HP:0030399
Impaired platelet adhesion

HP:0008352
Decreased platelet glycoprotein IIb-IIIa

HP:0001975
Abnormal platelet dense granule secretion

HP:0030397
Impaired ADP-induced platelet aggregation

HP:0004866
Abnormal platelet aggregation

HP:0030402
Macrothrombocytopenia

HP:0040185
Abnormal platelet ATP dense granule secretion

HP:0030398
Increased plasma vitamin K epoxide after vitamin K supplementation

HP:0040239
Decreased level of plasminogen

HP:0040228
Abnormal platelet function

HP:0011869
Hyperfibrinogenemia

HP:0011899
Decrease in high molecular weight von Willebrand factor Multimers

HP:0040225
Reduced factor IX activity

HP:0011858
Impaired ristocetin cofactor assay activity

HP:0030129
Decreased level of heparin co-factor II

HP:0040226
Abnormal surface-connected open canalicular system

HP:0012485
Reduced von Willebrand factor activity

HP:0008330
Heparin-induced thrombocytopenia

HP:0011874
Increased ratio of VWF propeptide to VWF antigen

HP:0040240
negative regulation of platelet-derived growth factor receptor-beta signaling pathway

GO:2000587
Prolonged whole-blood clotting time

HP:0005542
Post-transfusion thrombocytopenia

HP:0004813
Abnormal platelet shape

HP:0012524
Factor XIII subunit B deficiency

HP:0040234
regulation of platelet-derived growth factor receptor-beta signaling pathway

GO:2000586
positive regulation of prolactin signaling pathway

GO:1902213
Histoplasma capsulatum gastritis

DOID:0050225
Deviation of the 2nd finger

HP:0009468
Total absence von Willebrand factor multimers

HP:0030134
Decreased level of tissue plasminogen activator

HP:0040230
Absence of large von Willibrand factor multimers

HP:0030132
neural tube patterning

GO:0021532
Broad phalanges of the 3rd finger

HP:0009440
Decreased level of histidine-rich glycoprotein

HP:0040227
Distally placed thumb

HP:0009622
Abnormal dense tubular system

HP:0012491
Elevated factor V activity

HP:0011996
regulation of synaptic vesicle uncoating

GO:1903388
Neonatal alloimmune thrombocytopenia

HP:0004809
Transient hypogammaglobulinemia of infancy

HP:0005432
Fluctuations in consciousness

HP:0007159
Reduced factor XIII activity

HP:0008357
Ambiguous genitalia

HP:0000061
vulvar benign neoplasm

DOID:0060109
Ectopic anterior pituitary gland

HP:0012731
Reduced antithrombin antigen

HP:0040246
Small epiphyses of the distal phalanges of the hand

HP:0010254
Sclerosis of distal finger phalanx

HP:0100915
Absence of intermediate von Willibrand factor multimers

HP:0030135
Decreased urinary urate

HP:0011935
Broad phalanges of the 2nd finger

HP:0009547
Radial deviation of the 4th finger

HP:0009279
cerebral cortex tangential migration using cell-cell interactions

GO:0021823
regulation of L-glutamate import

GO:1900920
Fifth metacarpal with ulnar notch

HP:0005900
Lamellar cataract

HP:0007971
regulation of calcium ion-dependent exocytosis of neurotransmitter

GO:1903233
Reduced quantity of Von Willebrand factor

HP:0012147
Hypofibrinogenemia

HP:0011900
Sclerosis of the middle phalanx of the 5th finger

HP:0100907
negative regulation of humoral immune response

GO:0002921
Reduced euglobulin clot lysis time

HP:0040247
Lobular glomerulopathy

HP:0008636
progressive alteration of chromatin involved in cell aging

GO:0001301
Bracket epiphyses of the 4th finger

HP:0009394
fallopian tube benign neoplasm

DOID:0060111
Congenital thrombocytopenia

HP:0001905
Ileal atresia

HP:0011102
Bullet-shaped middle phalanx of the 4th finger

HP:0009296
larval foraging behavior

GO:0035177
Decreased marginal zone B cell count

HP:0030384
Decreased mean platelet volume

HP:0005537
Abnormal marginal zone B cell count

HP:0030383
Fragmentation of the epiphyses of the middle phalanges of the hand

HP:0010261
Absent epiphysis of the proximal phalanx of the 3rd finger

HP:0009346
Abnormal memory B cell count

HP:0030373
negative regulation of protein kinase-mediated signal transduction in response to host

GO:0075170
Post-partum hemorrhage

HP:0011891
Irregular epiphyses of the middle phalanges of the hand

HP:0010262
Lamellar pulverulent cataract

HP:0010694
EEG with focal sharp slow waves

HP:0011195
Abnormality of the proximal phalanx of the 2nd finger

HP:0009544
Enhanced ristocetin cofactor assay activity

HP:0030136
Broad middle phalanx of the 3rd finger

HP:0009430

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