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.
← Back to all clusters
Cluster 38
17
Diseases
80
Unique genes
0.278
Avg. similarity score
Cavernous hemangioma
Most-connected disease (14 links)
Disease
Searched: Hematopoietic and lymphoid cell neoplasm
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.
Hematopoietic and lymphoid cell neoplasm
Cavernous hemangioma
Extraskeletal ewing sarcoma
Skeletal ewing sarcoma
Osteochondroma
Askin tumor
Benign fibrous histiocytoma
Bleeding disorder, platelet-type, 21
Paris-trousseau thrombocytopenia
Ectomesenchymoma
Ewing sarcoma
Pineoblastoma
Spindle cell sarcoma
Osteogenic sarcoma
Congenital left-sided heart lesions
Angiomatoid fibrous histiocytoma
Tolchin-le caignec syndrome
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Cavernous hemangioma | 14 | 14 | 3 |
| Extraskeletal ewing sarcoma | 14 | 14 | 4 |
| Skeletal ewing sarcoma | 13 | 13 | 5 |
| Osteochondroma | 10 | 10 | 5 |
| Askin tumor | 9 | 9 | 5 |
| Benign fibrous histiocytoma | 6 | 6 | 1 |
| Bleeding disorder, platelet-type, 21 | 6 | 6 | 1 |
| Hematopoietic and lymphoid cell neoplasm | 6 | 6 | 8 |
| Paris-trousseau thrombocytopenia | 6 | 6 | 1 |
| Ectomesenchymoma | 5 | 5 | 7 |
| Ewing sarcoma | 5 | 5 | 10 |
| Pineoblastoma | 5 | 5 | 6 |
| Spindle cell sarcoma | 5 | 5 | 13 |
| Osteogenic sarcoma | 4 | 4 | 21 |
| Congenital left-sided heart lesions | 3 | 3 | 25 |
| Angiomatoid fibrous histiocytoma | 2 | 2 | 2 |
| Tolchin-le caignec syndrome | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| FLI1 | 15 / 17 | Askin tumor, Benign fibrous histiocytoma, Bleeding disorder, platelet-type, 21, Cavernous hemangioma and 11 more |
| EWSR1 | 12 / 17 | Angiomatoid fibrous histiocytoma, Askin tumor, Cavernous hemangioma, Ectomesenchymoma and 8 more |
| ERG | 10 / 17 | Askin tumor, Cavernous hemangioma, Ectomesenchymoma, Ewing sarcoma and 6 more |
| ETV1 | 2 / 17 | Ewing sarcoma, Skeletal ewing sarcoma |
| FUS | 2 / 17 | Askin tumor, Spindle cell sarcoma |
| LRP1B | 2 / 17 | Hematopoietic and lymphoid cell neoplasm, Osteogenic sarcoma |
| SOX6 | 2 / 17 | Osteochondroma, Tolchin-le caignec syndrome |
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 ⇵ |
|---|---|---|---|---|---|
| Prostate cancer | KEGG | 11 / 98 | 16.9× | 3.96e-11 | 5.23e-9 ✓ sig. |
| Non-small cell lung cancer | KEGG | 9 / 73 | 18.5× | 1.12e-9 | 1.03e-7 ✓ sig. |
| Transcriptional misregulation in cancer | KEGG | 12 / 198 | 9.1× | 6.53e-9 | 5.06e-7 ✓ sig. |
| Melanoma | KEGG | 8 / 73 | 16.5× | 2.57e-8 | 1.70e-6 ✓ sig. |
| Glioma | KEGG | 8 / 76 | 15.8× | 3.55e-8 | 2.26e-6 ✓ sig. |
| Chronic myeloid leukemia | KEGG | 8 / 77 | 15.6× | 3.94e-8 | 2.48e-6 ✓ sig. |
| Endometrial cancer | KEGG | 7 / 59 | 17.8× | 1.15e-7 | 6.33e-6 ✓ sig. |
| Hepatocellular carcinoma | KEGG | 10 / 170 | 8.8× | 1.74e-7 | 9.04e-6 ✓ sig. |
| Human T-cell leukemia virus 1 infection | KEGG | 11 / 224 | 7.4× | 2.52e-7 | 1.26e-5 ✓ sig. |
| Bladder cancer | KEGG | 6 / 41 | 22.0× | 2.70e-7 | 1.33e-5 ✓ sig. |
| Central carbon metabolism in cancer | KEGG | 7 / 71 | 14.8× | 4.21e-7 | 1.97e-5 ✓ sig. |
| Pathways in cancer | KEGG | 15 / 533 | 4.2× | 1.93e-6 | 7.32e-5 ✓ sig. |
| Longevity regulating pathway | KEGG | 7 / 90 | 11.7× | 2.14e-6 | 8.00e-5 ✓ sig. |
| Endocrine resistance | KEGG | 7 / 99 | 10.6× | 4.06e-6 | 1.38e-4 ✓ sig. |
| Breast cancer | KEGG | 8 / 148 | 8.1× | 6.03e-6 | 1.92e-4 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| regulation of DNA-templated transcription | GO:0006355 | 25 / 1,454 | 4.0× | 8.51e-10 | 2.02e-7 ✓ sig. |
| regulation of transcription by RNA polymerase II | GO:0006357 | 26 / 1,602 | 3.8× | 1.21e-9 | 2.73e-7 ✓ sig. |
| positive regulation of transcription by RNA polymerase II | GO:0045944 | 22 / 1,208 | 4.3× | 4.08e-9 | 8.00e-7 ✓ sig. |
| positive regulation of DNA-templated transcription | GO:0045893 | 17 / 778 | 5.1× | 2.47e-8 | 3.88e-6 ✓ sig. |
| regulation of cell cycle | GO:0051726 | 9 / 262 | 8.0× | 1.78e-6 | 1.38e-4 ✓ sig. |
| regulation of G1/S transition of mitotic cell cycle | GO:2000045 | 5 / 57 | 20.5× | 4.46e-6 | 2.89e-4 ✓ sig. |
| epidermal growth factor receptor signaling pathway | GO:0007173 | 5 / 64 | 18.2× | 7.93e-6 | 4.55e-4 ✓ sig. |
| cAMP/PKA signal transduction | GO:0141156 | 3 / 10 | 70.1× | 8.87e-6 | 4.95e-4 ✓ sig. |
| learning or memory | GO:0007611 | 5 / 72 | 16.2× | 1.42e-5 | 7.13e-4 ✓ sig. |
| negative regulation of DNA-templated transcription | GO:0045892 | 12 / 631 | 4.4× | 1.46e-5 | 7.30e-4 ✓ sig. |
| positive regulation of hormone secretion | GO:0046887 | 3 / 12 | 58.4× | 1.62e-5 | 7.89e-4 ✓ sig. |
| regulation of cell population proliferation | GO:0042127 | 7 / 201 | 8.1× | 2.45e-5 | 1.08e-3 ✓ sig. |
| replicative senescence | GO:0090399 | 3 / 16 | 43.8× | 4.06e-5 | 1.57e-3 ✓ sig. |
| positive regulation of Schwann cell differentiation | GO:0014040 | 2 / 3 | 156× | 5.41e-5 | 1.96e-3 ✓ sig. |
| regulation of centromere complex assembly | GO:0090230 | 2 / 3 | 156× | 5.41e-5 | 1.96e-3 ✓ sig. |