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.

Elevated factor V activity

ID: HP:0011996

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

Label: Elevated factor V activity

Synonyms: Elevated factor V activity

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Elevated factor V activity

HP:0011996
Decreased level of histidine-rich glycoprotein

HP:0040227
Factor X activation deficiency

HP:0008354
Factor XIII subunit B deficiency

HP:0040234
Decreased level of plasminogen

HP:0040228
Total absence von Willebrand factor multimers

HP:0030134
Decreased level of tissue plasminogen activator

HP:0040230
Enhanced ristocetin cofactor assay activity

HP:0030136
Increased plasma vitamin K epoxide after vitamin K supplementation

HP:0040239
Reduced factor XIII activity

HP:0008357
Reduced prothrombin consumption

HP:0003337
Hyperfibrinogenemia

HP:0011899
Decreased level of heparin co-factor II

HP:0040226
Reduced factor IX activity

HP:0011858
Factor XIII subunit A deficiency

HP:0040233
Hypofibrinogenemia

HP:0011900
Dysfibrinogenemia

HP:0011901
Reduced antithrombin antigen

HP:0040246
Prolonged Russell'\''s viper venom time

HP:0040244
Reduced von Willebrand factor activity

HP:0008330
Reduced alpha-2-antiplasmin activity

HP:0040245
Reduced antithrombin III activity

HP:0001976
Impaired binding of factor VIII to VWF

HP:0040237
Decreased level of thrombomodulin

HP:0040229
Reduced euglobulin clot lysis time

HP:0040247
Absence of large von Willibrand factor multimers

HP:0030132
Abnormality of circulating fibrinogen

HP:0011898
Impaired ristocetin-induced platelet aggregation

HP:0011871
Impaired von Willibrand factor collagen binding activity

HP:0030130
Reduced quantity of Von Willebrand factor

HP:0012147
Abnormal presence of ultra-large von Willebrand factor multimers

HP:0030133
Hyperfibrinolysis

HP:0040236
Exaggerated cellular immune processes

HP:0005397
Absence of intermediate von Willibrand factor multimers

HP:0030135
Reduced kininogen activity

HP:0005527
Reduced factor VIII activity

HP:0003125
EEG with 4-5/second background activity

HP:0011177
Abnormality of fibrinolysis

HP:0040224
Abnormal alpha-beta T cell morphology

HP:0030333
Increased ratio of VWF propeptide to VWF antigen

HP:0040240
Abnormality of the kinin-kallikrein system

HP:0005559
Impaired ristocetin cofactor assay activity

HP:0030129
Abnormal marginal zone B cell count

HP:0030383
Onychogryposis of fingernail

HP:0040036
Decreased T cell activation

HP:0005419
Decreased marginal zone B cell count

HP:0030384
Reduced plasminogen activator inhibitor 1 activity

HP:0040248
Widened cerebellar subarachnoid space

HP:0012765
Reduced factor V activity

HP:0003225
Absent natural killer cells

HP:0040219
regulation of B cell antigen processing and presentation

GO:0002622
no_name

GO:0043340
Defective B cell activation

HP:0005384
Abnormal von Willebrand factor multimer distribution

HP:0030131
establishment of planar polarity involved in nephron morphogenesis

GO:0072046
Abnormality of von Willebrand factor

HP:0012146
Prolonged whole-blood clotting time

HP:0005542
Low voltage EEG

HP:0011181
Impaired arachidonic acid-induced platelet aggregation

HP:0011870
Reduced circulating T-helper cells

HP:0008165
Reduced factor XII activity

HP:0004841
Decrease in high molecular weight von Willebrand factor Multimers

HP:0040225
Resistance to activated protein C

HP:0012175
obsolete cytoplasmic dynein light chain

GO:0001690
Increased laxity of fingers

HP:0006149
Abnormal muscle fiber emerin

HP:0030116
Hypermobility of interphalangeal joints

HP:0005620
Defective B cell differentiation

HP:0005357
Post-partum hemorrhage

HP:0011891
Reduced factor X activity

HP:0008321
establishment of body hair or bristle planar orientation

GO:0048104
Abnormal CD4-positive

HP:0030334
Abnormality of the common coagulation pathway

HP:0010990
Abnormal insertion of umbilical cord

HP:0011418
Reduced factor XI activity

HP:0001929
Chronic CSF lymphocytosis

HP:0009704
type 1 somatostatin receptor binding

GO:0031878
EEG with persistent abnormal rhythmic activity

HP:0010846
Decreased number of CD4+ T cells

HP:0005407
Contracture of the metacarpophalangeal joint of the 3rd finger

HP:0009470
Abnormality of the deltoid tuberosities

HP:0003889
no_name

GO:0008844
2-hydroxyisoflavanone dehydratase activity

GO:0033987
Ectopic anterior pituitary gland

HP:0012731
Abnormal fucosylation of protein N-linked glycosylation

HP:0012352
anaplastic secondary supratentorial astrocytic neoplasm

DOID:8146
Reduced plasminogen activator inhibitor 1 antigen

HP:0040249
Arterial disease of legs

HP:0005794
Hypersegmentation of neutrophil nuclei

HP:0004821
Onycholysis of fingernails

HP:0040039
Decreased fucosylation of N-linked protein glycosylation

HP:0012353
Abnormal level of neopterin

HP:0040206
no_name

GO:0042526
Increased marginal zone B cell count

HP:0030385
positive regulation of transcription from RNA polymerase II promoter in response to maltose

GO:1904765
High nonceruloplasmin-bound serum copper

HP:0010838
maintenance of dauer

GO:0043055
establishment of thoracic bristle planar orientation

GO:0048106
Impaired thrombin-induced platelet aggregation

HP:0011872
HbS hemoglobin

HP:0045047

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