Disease Clusters?
Groups of diseases that share a large number of curated genes with each other, computed via label propagation over the shared-gene similarity graph. See also Shared-Gene Disease Pairs for pairwise comparisons.
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Cluster 29
19
Diseases
37
Unique genes
0.330
Avg. similarity score
Cholesterol embolism
Most-connected disease (11 links)
Disease
Pinned (dragged)
Node size = connections within this cluster · edge thickness = similarity strength · hover an edge for its details ·
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Cholesterol embolism
Aphasia
Intracranial embolism and thrombosis
Postictal aphasia
Cardiac tamponade
Commisural aphasia
Dejerine-lichtheim phenomenon
Arterial occlusive disease
Brain edema
Dysphasia
Spinal cord compression
Syntactic aphasia
Cardiac injury
Hematoma
Intracranial hemorrhage
quebec platelet disorder
Asthenozoospermia
Hepatic lipase deficiency
dilated cardiomyopathy 1D
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Cholesterol embolism | 11 | 11 | 2 |
| Aphasia | 10 | 10 | 2 |
| Intracranial embolism and thrombosis | 10 | 10 | 2 |
| Postictal aphasia | 9 | 9 | 2 |
| Cardiac tamponade | 8 | 8 | 1 |
| Commisural aphasia | 6 | 6 | 2 |
| Dejerine-lichtheim phenomenon | 6 | 6 | 2 |
| Arterial occlusive disease | 5 | 5 | 9 |
| Brain edema | 5 | 5 | 10 |
| Dysphasia | 5 | 5 | 4 |
| Spinal cord compression | 5 | 5 | 3 |
| Syntactic aphasia | 5 | 5 | 2 |
| Cardiac injury | 4 | 4 | 4 |
| Hematoma | 4 | 4 | 3 |
| Intracranial hemorrhage | 4 | 4 | 13 |
| quebec platelet disorder | 4 | 4 | 1 |
| Asthenozoospermia | 3 | 3 | 3 |
| Hepatic lipase deficiency | 1 | 1 | 1 |
| dilated cardiomyopathy 1D | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| PLAT | 14 / 19 | Aphasia, Arterial occlusive disease, Brain edema, Cardiac tamponade and 10 more |
| PLAU | 8 / 19 | Arterial occlusive disease, Asthenozoospermia, Brain edema, Cardiac injury and 4 more |
| L1CAM | 6 / 19 | Aphasia, Commisural aphasia, Dejerine-lichtheim phenomenon, Dysphasia and 2 more |
| F7 | 2 / 19 | Hematoma, Intracranial hemorrhage |
| LIPC | 2 / 19 | Arterial occlusive disease, Hepatic lipase deficiency |
| S100B | 2 / 19 | Brain edema, Hematoma |
| TNF | 2 / 19 | Brain edema, Spinal cord compression |
| TNNT2 | 2 / 19 | Cardiac injury, dilated cardiomyopathy 1D |
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 ⇵ |
|---|---|---|---|---|---|
| Interleukin-4 and Interleukin-13 signaling | Reactome | 5 / 108 | 15.0× | 1.86e-5 | 5.64e-4 ✓ sig. |
| TNF signaling pathway | KEGG | 5 / 119 | 13.6× | 2.97e-5 | 8.27e-4 ✓ sig. |
| Fluid shear stress and atherosclerosis | KEGG | 5 / 141 | 11.5× | 6.69e-5 | 1.62e-3 ✓ sig. |
| Complement and coagulation cascades | KEGG | 4 / 88 | 14.8× | 1.48e-4 | 3.08e-3 ✓ sig. |
| IL-17 signaling pathway | KEGG | 4 / 94 | 13.8× | 1.91e-4 | 3.77e-3 ✓ sig. |
| Chagas disease | KEGG | 4 / 103 | 12.6× | 2.71e-4 | 4.96e-3 ✓ sig. |
| Interleukin-10 signaling | Reactome | 3 / 47 | 20.7× | 3.98e-4 | 6.68e-3 ✓ sig. |
| Malaria | KEGG | 3 / 50 | 19.5× | 4.78e-4 | 7.69e-3 ✓ sig. |
| Lipid and atherosclerosis | KEGG | 5 / 216 | 7.5× | 4.90e-4 | 7.85e-3 ✓ sig. |
| Eicosanoids | Reactome | 2 / 12 | 54.1× | 5.98e-4 | 9.16e-3 ✓ sig. |
| Dissolution of Fibrin Clot | Reactome | 2 / 13 | 49.9× | 7.05e-4 | 1.04e-2 ✓ sig. |
| Fatty acids | Reactome | 2 / 15 | 43.3× | 9.46e-4 | 1.30e-2 ✓ sig. |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | Reactome | 2 / 20 | 32.5× | 1.69e-3 | 2.02e-2 ✓ sig. |
| Pertussis | KEGG | 3 / 78 | 12.5× | 1.75e-3 | 2.07e-2 ✓ sig. |
| RHO GTPases activate PAKs | Reactome | 2 / 23 | 28.2× | 2.24e-3 | 2.48e-2 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| cellular response to lipopolysaccharide | GO:0071222 | 7 / 187 | 18.9× | 7.17e-8 | 9.13e-6 ✓ sig. |
| response to hypoxia | GO:0001666 | 6 / 176 | 17.2× | 1.17e-6 | 9.40e-5 ✓ sig. |
| plasminogen activation | GO:0031639 | 3 / 12 | 126× | 1.55e-6 | 1.18e-4 ✓ sig. |
| negative regulation of fibrinolysis | GO:0051918 | 3 / 12 | 126× | 1.55e-6 | 1.18e-4 ✓ sig. |
| regulation of muscle contraction | GO:0006937 | 3 / 16 | 94.7× | 3.93e-6 | 2.48e-4 ✓ sig. |
| positive regulation of glial cell proliferation | GO:0060252 | 3 / 22 | 68.9× | 1.07e-5 | 5.50e-4 ✓ sig. |
| response to genistein | GO:0033595 | 2 / 3 | 337× | 1.14e-5 | 5.77e-4 ✓ sig. |
| regulation of fibrinolysis | GO:0051917 | 2 / 4 | 253× | 2.28e-5 | 9.94e-4 ✓ sig. |
| response to 2,3,7,8-tetrachlorodibenzodioxine | GO:1904612 | 2 / 5 | 202× | 3.80e-5 | 1.46e-3 ✓ sig. |
| menaquinone catabolic process | GO:0042361 | 2 / 5 | 202× | 3.80e-5 | 1.46e-3 ✓ sig. |
| vascular endothelial growth factor production | GO:0010573 | 2 / 6 | 168× | 5.69e-5 | 1.98e-3 ✓ sig. |
| phylloquinone catabolic process | GO:0042376 | 2 / 6 | 168× | 5.69e-5 | 1.98e-3 ✓ sig. |
| negative regulation of plasminogen activation | GO:0010757 | 2 / 7 | 144× | 7.96e-5 | 2.55e-3 ✓ sig. |
| regulation of insulin secretion | GO:0050796 | 3 / 46 | 32.9× | 1.02e-4 | 3.07e-3 ✓ sig. |
| very-low-density lipoprotein particle remodeling | GO:0034372 | 2 / 8 | 126× | 1.06e-4 | 3.16e-3 ✓ sig. |