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Cluster 36

17 diseases · 38 shared-gene connections
17 Diseases
281 Unique genes
0.109 Avg. similarity score
Thrombosis Most-connected disease (11 links)
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Disease Pinned (dragged)
Node size = connections within this cluster · edge thickness = similarity strength · hover an edge for its details · click a node to select it and show its pairs below (double-click or Ctrl/⌘-click opens the disease page) · drag a node to pin it in place · scroll/pinch to zoom.

Member diseases (most connected first ‐ the cluster's core)

Top shared genes (genes linked to 2+ member diseases)

Gene ⇵ Member diseases ⇵ Linked diseases
F2 9 / 17 Blood coagulation disorder, Disseminated intravascular coagulation, Hemophilia a, Hemorrhage and 5 more
PLAT 9 / 17 Cerebral hemorrhage, Hemophilia a, Hemorrhage, Ischemic stroke and 5 more
F7 8 / 17 Cerebral hemorrhage, Disseminated intravascular coagulation, Hemorrhage, Hemorrhagic disease and 4 more
PROC 7 / 17 Blood coagulation disorder, Disseminated intravascular coagulation, Ischemic stroke, Thromboembolism and 3 more
F5 6 / 17 Blood coagulation disorder, Ischemic stroke, Thromboembolism, Thrombophilia and 2 more
MTHFR 6 / 17 Blood coagulation disorder, Hemophilia a, Ischemic stroke, Thrombocytopenia and 2 more
PLAU 6 / 17 Cerebral hemorrhage, Hemorrhage, Ischemic stroke, Thromboembolism and 2 more
SERPINC1 6 / 17 Blood coagulation disorder, Cerebral hemorrhage, Disseminated intravascular coagulation, Thrombocytopenia and 2 more
THBD 6 / 17 Disseminated intravascular coagulation, Ischemic stroke, Thrombocytopenia, Thrombomodulin-related bleeding disorder and 2 more
PROS1 5 / 17 Ischemic stroke, Thrombocytopenia, Thromboembolism, Thrombophilia and 1 more
F13A1 4 / 17 Disseminated intravascular coagulation, Thrombocytopenia, Thrombophilia, Venous thrombosis
F3 4 / 17 Disseminated intravascular coagulation, Spontaneous coronary artery dissection, Thrombosis, Venous thrombosis
FCGR2A 4 / 17 Fetal erythroblastosis, Hemophilia a, Thrombocytopenia, Thrombosis
HMOX1 4 / 17 Blood coagulation disorder, Cerebral hemorrhage, Hemophilia a, Thrombosis
JAK2 4 / 17 Hemorrhagic disease, Thrombocytopenia, Thromboembolism, Venous thrombosis
TFPI 4 / 17 Disseminated intravascular coagulation, Hemophilia a, Thrombophilia, Venous thrombosis
EPO 3 / 17 Thrombocytopenia, Thrombosis, Venous thrombosis
F10 3 / 17 Blood coagulation disorder, Thrombocytopenia, Thrombosis
F8 3 / 17 Hemophilia a, Thrombophilia, Venous thrombosis
F9 3 / 17 Hemophilia a, Thrombophilia, Thrombosis
FGA 3 / 17 Thrombocytopenia, Thrombophilia, Thrombosis
FGG 3 / 17 Blood coagulation disorder, Thrombocytopenia, Thrombophilia
ITGB3 3 / 17 Cerebral hemorrhage, Hemorrhage, Thrombocytopenia
LPA 3 / 17 Thrombocytopenia, Thromboembolism, Venous thrombosis
MERTK 3 / 17 MERTK-related retinopathy, Thromboembolism, Thrombosis
P2RY12 3 / 17 Hemorrhage, Thrombocytopenia, Thrombosis
PLG 3 / 17 Thrombocytopenia, Thrombophilia, Venous thrombosis
TNF 3 / 17 Ischemic stroke, Thrombocytopenia, Thrombosis
VKORC1 3 / 17 Blood coagulation disorder, Hemorrhage, Thrombosis
VWF 3 / 17 Hemophilia a, Thrombocytopenia, Thrombosis
ABO 2 / 17 Blood coagulation disorder, Thrombophilia
ACE 2 / 17 Cerebral hemorrhage, Ischemic stroke
ACVRL1 2 / 17 Hemophilia a, Thrombocytopenia
ARHGEF3 2 / 17 Hemorrhagic disease, Thrombocytopenia
ATP1B1 2 / 17 Blood coagulation disorder, Thrombophilia
BAK1 2 / 17 Hemorrhagic disease, Thrombocytopenia
BDKRB2 2 / 17 Hemorrhage, Thrombosis
CDKN2A 2 / 17 Hemorrhagic disease, Thrombocytopenia
CSF2 2 / 17 Thrombocytopenia, Venous thrombosis
F11 2 / 17 Thrombocytopenia, Thrombophilia
FGB 2 / 17 Thrombocytopenia, Thrombophilia
GAS6 2 / 17 Thromboembolism, Thrombosis
GCSAML 2 / 17 Hemorrhagic disease, Thrombocytopenia
GGCX 2 / 17 Blood coagulation disorder, Thrombocytopenia
GP1BA 2 / 17 Thrombocytopenia, Thrombosis
GTF3C5 2 / 17 Hemorrhagic disease, Thrombocytopenia
HBS1L 2 / 17 Hemorrhagic disease, Thrombocytopenia
HLA-A 2 / 17 Ischemic stroke, Thrombocytopenia
HLA-DQA1 2 / 17 Hemophilia a, Thrombophilia
HRG 2 / 17 hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency, Thrombophilia
IL10 2 / 17 Hemophilia a, Thrombocytopenia
ITGA2B 2 / 17 Cerebral hemorrhage, Thrombocytopenia
JMJD1C 2 / 17 Hemorrhagic disease, Thrombocytopenia
KDR 2 / 17 Cerebral hemorrhage, Venous thrombosis
KLKB1 2 / 17 Thrombocytopenia, Thrombosis
MMP2 2 / 17 Cerebral hemorrhage, Ischemic stroke
MMP9 2 / 17 Cerebral hemorrhage, Ischemic stroke
NME7 2 / 17 Blood coagulation disorder, Thrombophilia
PF4 2 / 17 Thrombocytopenia, Thrombosis
PNPLA3 2 / 17 Hemorrhagic disease, Thrombocytopenia
PODXL 2 / 17 Hemorrhage, Thrombosis
POMC 2 / 17 Cerebral hemorrhage, Hemorrhage
SERPINA1 2 / 17 Hemorrhage, Hemorrhagic disease
SERPINA10 2 / 17 Thrombophilia, Venous thrombosis
SIRPA 2 / 17 Hemorrhagic disease, Thrombocytopenia
SLC19A2 2 / 17 Blood coagulation disorder, Thrombophilia
STXBP2 2 / 17 Hemorrhage, Thrombocytopenia
TBXAS1 2 / 17 Ischemic stroke, Thrombocytopenia
THADA 2 / 17 Hemorrhagic disease, Thrombocytopenia
THPO 2 / 17 Hemorrhagic disease, Thrombocytopenia
TPM4 2 / 17 Hemorrhagic disease, Thrombocytopenia
TUBB1 2 / 17 Hemorrhagic disease, Thrombocytopenia
VEGFA 2 / 17 Cerebral hemorrhage, Hemorrhage
ZNF474 2 / 17 Hemorrhagic disease, Thrombocytopenia
ZNF475 2 / 17 Hemorrhagic disease, Thrombocytopenia
What do these columns mean?
Connections in cluster
How many other members this disease has a shared-gene link to (the node size in the network above). The most-connected diseases are the cluster's core.
Significant partners
How many of those links are statistically significant (FDR q < 0.05).
Curated genes
Distinct curated genes linked to that disease in GeDiPNet.
Member diseases (Top shared genes)
How many of this cluster's diseases are linked to the gene, out of the cluster's total. Genes shared by many members are the most direct explanation of why they group together.
Overlap genes (x / y)
x = genes shared between this cluster and the pathway/GO term; y = that pathway/GO term's total gene count. A higher x relative to y (and to the cluster's own size) means a tighter biological match.
Cluster gene count
Total distinct genes across every disease in this cluster -- the "n" used in the significance test below.
Fold enrichment
Observed overlap divided by the overlap expected by chance, given the cluster's gene count, the pathway/term's size and the gene universe tested. 5× means five times more shared genes than random. Tells strong hits apart when q-values are all vanishingly small.
P-value / FDR q-value
Is this pathway/GO term's overlap with the cluster more than chance? Upper-tail hypergeometric test, Benjamini-Hochberg corrected across every tested pathway/term (prefer the q-value -- it accounts for testing many at once).
Shared genes (Pairs within this cluster)
Number of curated genes the two diseases in that row have in common.
Similarity score (Pairs within this cluster)
Jaccard-based gene overlap between the two specific diseases in that row -- same metric as the main Shared-Gene Disease Pairs page.

Enriched Pathways (why this cluster is grouped, biologically)

Pathway ⇵ Source ⇵ Overlap genes ⇵ Fold enrichment ⇵ P-value ⇵ FDR q-value ⇵
Complement and coagulation cascades KEGG 30 / 88 14.6× 2.24e-27 5.26e-24 ✓ sig.
Platelet degranulation Reactome 31 / 123 10.8× 9.35e-24 1.36e-20 ✓ sig.
Intrinsic Pathway of Fibrin Clot Formation Reactome 16 / 23 29.7× 1.12e-21 1.17e-18 ✓ sig.
Platelet activation KEGG 29 / 126 9.8× 4.45e-21 4.31e-18 ✓ sig.
Common Pathway of Fibrin Clot Formation Reactome 15 / 22 29.1× 3.50e-20 2.76e-17 ✓ sig.
Pathways in cancer KEGG 45 / 533 3.6× 4.19e-14 1.13e-11 ✓ sig.
Gamma-carboxylation of protein precursors Reactome 8 / 9 38.0× 7.18e-13 1.61e-10 ✓ sig.
Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus Reactome 8 / 9 38.0× 7.18e-13 1.61e-10 ✓ sig.
AGE-RAGE signaling pathway in diabetic complications KEGG 19 / 101 8.0× 1.64e-12 3.45e-10 ✓ sig.
Removal of aminoterminal propeptides from gamma-carboxylated proteins Reactome 8 / 10 34.2× 3.52e-12 6.87e-10 ✓ sig.
Integrin cell surface interactions Reactome 17 / 81 9.0× 3.90e-12 7.54e-10 ✓ sig.
Interleukin-4 and Interleukin-13 signaling Reactome 19 / 108 7.5× 5.72e-12 1.08e-9 ✓ sig.
p130Cas linkage to MAPK signaling for integrins Reactome 9 / 15 25.6× 8.19e-12 1.50e-9 ✓ sig.
GRB2:SOS provides linkage to MAPK signaling for Integrins Reactome 9 / 15 25.6× 8.19e-12 1.50e-9 ✓ sig.
Hematopoietic cell lineage KEGG 18 / 100 7.7× 1.40e-11 2.43e-9 ✓ sig.

Enriched GO Terms (Biological Process, a second line of biological evidence)

GO term ⇵ GO ID ⇵ Overlap genes ⇵ Fold enrichment ⇵ P-value ⇵ FDR q-value ⇵
blood coagulation GO:0007596 51 / 106 32.0× 2.74e-65 1.79e-60 ✓ sig.
hemostasis GO:0007599 38 / 55 45.9× 2.24e-57 6.53e-53 ✓ sig.
fibrinolysis GO:0042730 14 / 19 49.0× 2.38e-22 5.33e-19 ✓ sig.
platelet activation GO:0030168 18 / 69 17.3× 7.76e-18 9.10e-15 ✓ sig.
platelet aggregation GO:0070527 16 / 49 21.7× 9.56e-18 1.12e-14 ✓ sig.
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction GO:0051897 27 / 217 8.3× 2.83e-17 3.04e-14 ✓ sig.
platelet formation GO:0030220 12 / 24 33.3× 2.43e-16 2.14e-13 ✓ sig.
megakaryocyte development GO:0035855 10 / 23 28.9× 4.85e-13 2.37e-10 ✓ sig.
positive regulation of ERK1 and ERK2 cascade GO:0070374 20 / 201 6.6× 2.79e-11 9.11e-9 ✓ sig.
plasminogen activation GO:0031639 7 / 12 38.8× 1.20e-10 3.38e-8 ✓ sig.
negative regulation of fibrinolysis GO:0051918 7 / 12 38.8× 1.20e-10 3.38e-8 ✓ sig.
positive regulation of platelet activation GO:0010572 7 / 13 35.8× 2.56e-10 6.65e-8 ✓ sig.
blood coagulation, intrinsic pathway GO:0007597 6 / 8 49.9× 2.99e-10 7.65e-8 ✓ sig.
angiogenesis GO:0001525 22 / 284 5.2× 3.73e-10 9.24e-8 ✓ sig.
blood coagulation, fibrin clot formation GO:0072378 6 / 9 44.3× 8.87e-10 2.01e-7 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Hemorrhagic disease Thrombocytopenia 0.118 17 3.71e-32 1.29e-30 ✓ sig.
Thrombophilia Venous thrombosis 0.222 10 1.99e-22 4.46e-21 ✓ sig.
Thromboembolism Venous thrombosis 0.296 8 2.02e-21 4.30e-20 ✓ sig.
Disseminated intravascular coagulation Venous thrombosis 0.280 7 1.51e-19 2.95e-18 ✓ sig.
Blood coagulation disorder Thrombophilia 0.188 9 2.69e-19 5.18e-18 ✓ sig.
Thromboembolism Thrombosis 0.160 8 1.35e-18 2.53e-17 ✓ sig.
Thrombocytopenia Thrombosis 0.082 14 1.61e-18 3.00e-17 ✓ sig.
Thrombosis Venous thrombosis 0.133 8 8.55e-16 1.36e-14 ✓ sig.
Hemophilia a Thrombophilia 0.167 7 9.35e-16 1.48e-14 ✓ sig.
Thrombocytopenia Venous thrombosis 0.066 10 1.53e-15 2.39e-14 ✓ sig.
Ischemic stroke Thromboembolism 0.123 7 2.23e-15 3.43e-14 ✓ sig.
Thrombophilia Thrombosis 0.114 8 2.75e-14 3.95e-13 ✓ sig.
Hemorrhage Thrombosis 0.111 7 3.72e-13 4.94e-12 ✓ sig.
Blood coagulation disorder Thrombosis 0.111 7 3.72e-13 4.94e-12 ✓ sig.
Ischemic stroke Venous thrombosis 0.104 7 4.68e-13 6.17e-12 ✓ sig.
Ischemic stroke Thrombosis 0.090 8 1.60e-12 2.02e-11 ✓ sig.
Cerebral hemorrhage Hemorrhage 0.125 6 3.38e-12 4.08e-11 ✓ sig.
Disseminated intravascular coagulation Thrombophilia 0.135 5 3.50e-12 4.22e-11 ✓ sig.
Ischemic stroke Thrombophilia 0.091 7 9.00e-12 1.05e-10 ✓ sig.
Hemophilia a Venous thrombosis 0.147 5 1.58e-11 1.81e-10 ✓ sig.
Blood coagulation disorder Venous thrombosis 0.119 5 1.53e-10 1.58e-9 ✓ sig.
Cerebral hemorrhage Venous thrombosis 0.106 5 4.24e-10 4.22e-9 ✓ sig.
Hemorrhage Thromboembolism 0.121 4 2.23e-9 2.05e-8 ✓ sig.
Disseminated intravascular coagulation Thromboembolism 0.158 3 3.03e-8 2.42e-7 ✓ sig.
Hemorrhage Venous thrombosis 0.093 4 3.26e-8 2.59e-7 ✓ sig.
Blood coagulation disorder Disseminated intravascular coagulation 0.097 3 2.78e-7 1.91e-6 ✓ sig.
Hemorrhagic disease Thromboembolism 0.063 2 1.16e-4 3.90e-4 ✓ sig.
Disseminated intravascular coagulation Spontaneous coronary artery dissection 0.100 1 5.84e-4 1.14e-3 ✓ sig.
Disseminated intravascular coagulation Thrombomodulin-related bleeding disorder 0.100 1 5.84e-4 1.14e-3 ✓ sig.
MERTK-related retinopathy Thromboembolism 0.077 1 7.79e-4 1.39e-3 ✓ sig.
Spontaneous coronary artery dissection Venous thrombosis 0.043 1 1.43e-3 2.21e-3 ✓ sig.
Fetal erythroblastosis Hemophilia a 0.056 1 2.08e-3 2.95e-3 ✓ sig.
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Thrombophilia 0.030 1 2.08e-3 2.95e-3 ✓ sig.
Thrombomodulin-related bleeding disorder Thrombophilia 0.030 1 2.08e-3 2.95e-3 ✓ sig.
MERTK-related retinopathy Thrombosis 0.022 1 2.92e-3 3.87e-3 ✓ sig.
Spontaneous coronary artery dissection Thrombosis 0.022 1 2.92e-3 3.87e-3 ✓ sig.
Thrombomodulin-related bleeding disorder Thrombosis 0.022 1 2.92e-3 3.87e-3 ✓ sig.
Fetal erythroblastosis Thrombosis 0.021 1 5.84e-3 7.05e-3 ✓ sig.