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 184
8
Diseases
30
Unique genes
0.068
Avg. similarity score
Agammaglobulinemia
Most-connected disease (7 links)
Disease
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Agammaglobulinemia
Burkitt lymphoma
autosomal agammaglobulinemia
agammaglobulinemia 10, autosomal dominant
agammaglobulinemia 2, autosomal recessive
agammaglobulinemia 3, autosomal recessive
agammaglobulinemia 4, autosomal recessive
agammaglobulinemia 6, autosomal recessive
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Agammaglobulinemia | 7 | 7 | 13 |
| Burkitt lymphoma | 2 | 2 | 19 |
| autosomal agammaglobulinemia | 2 | 2 | 1 |
| agammaglobulinemia 10, autosomal dominant | 1 | 1 | 1 |
| agammaglobulinemia 2, autosomal recessive | 1 | 1 | 1 |
| agammaglobulinemia 3, autosomal recessive | 1 | 1 | 1 |
| agammaglobulinemia 4, autosomal recessive | 1 | 1 | 1 |
| agammaglobulinemia 6, autosomal recessive | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| TCF3 | 3 / 8 | Agammaglobulinemia, autosomal agammaglobulinemia, Burkitt lymphoma |
| BLNK | 2 / 8 | Agammaglobulinemia, agammaglobulinemia 4, autosomal recessive |
| CD79A | 2 / 8 | Agammaglobulinemia, agammaglobulinemia 3, autosomal recessive |
| CD79B | 2 / 8 | Agammaglobulinemia, agammaglobulinemia 6, autosomal recessive |
| IGLL1 | 2 / 8 | Agammaglobulinemia, agammaglobulinemia 2, autosomal recessive |
| PIK3R1 | 2 / 8 | Agammaglobulinemia, Burkitt lymphoma |
| SPI1 | 2 / 8 | Agammaglobulinemia, agammaglobulinemia 10, autosomal dominant |
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 ⇵ |
|---|---|---|---|---|---|
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | Reactome | 5 / 23 | 87.0× | 2.23e-9 | 2.27e-7 ✓ sig. |
| Acute myeloid leukemia | KEGG | 5 / 68 | 29.4× | 6.40e-7 | 3.31e-5 ✓ sig. |
| B cell receptor signaling pathway | KEGG | 5 / 91 | 22.0× | 2.74e-6 | 1.15e-4 ✓ sig. |
| Human T-cell leukemia virus 1 infection | KEGG | 6 / 224 | 10.7× | 1.61e-5 | 4.98e-4 ✓ sig. |
| Signaling pathways regulating pluripotency of stem cells | KEGG | 5 / 144 | 13.9× | 2.59e-5 | 7.36e-4 ✓ sig. |
| Central carbon metabolism in cancer | KEGG | 4 / 71 | 22.6× | 2.74e-5 | 7.71e-4 ✓ sig. |
| Pathways in cancer | KEGG | 8 / 533 | 6.0× | 3.51e-5 | 9.54e-4 ✓ sig. |
| Chronic myeloid leukemia | KEGG | 4 / 77 | 20.8× | 3.77e-5 | 1.01e-3 ✓ sig. |
| Hepatocellular carcinoma | KEGG | 5 / 170 | 11.8× | 5.73e-5 | 1.43e-3 ✓ sig. |
| CD22 mediated BCR regulation | Reactome | 2 / 5 | 160× | 6.00e-5 | 1.48e-3 ✓ sig. |
| Colorectal cancer | KEGG | 4 / 87 | 18.4× | 6.10e-5 | 1.50e-3 ✓ sig. |
| Interleukin-7 signaling | Reactome | 3 / 33 | 36.4× | 7.30e-5 | 1.73e-3 ✓ sig. |
| Primary immunodeficiency | KEGG | 3 / 38 | 31.6× | 1.12e-4 | 2.46e-3 ✓ sig. |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | Reactome | 3 / 38 | 31.6× | 1.12e-4 | 2.46e-3 ✓ sig. |
| Transcriptional misregulation in cancer | KEGG | 5 / 198 | 10.1× | 1.18e-4 | 2.56e-3 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| B cell differentiation | GO:0030183 | 7 / 80 | 54.5× | 3.79e-11 | 1.20e-8 ✓ sig. |
| B cell receptor signaling pathway | GO:0050853 | 4 / 56 | 44.5× | 1.87e-6 | 1.36e-4 ✓ sig. |
| positive regulation of DNA-templated transcription | GO:0045893 | 8 / 778 | 6.4× | 2.25e-5 | 9.86e-4 ✓ sig. |
| transcription initiation-coupled chromatin remodeling | GO:0045815 | 3 / 41 | 45.6× | 3.82e-5 | 1.47e-3 ✓ sig. |
| B cell activation | GO:0042113 | 3 / 44 | 42.5× | 4.73e-5 | 1.72e-3 ✓ sig. |
| myeloid leukocyte differentiation | GO:0002573 | 2 / 7 | 178× | 5.21e-5 | 1.86e-3 ✓ sig. |
| positive regulation of myoblast differentiation | GO:0045663 | 3 / 47 | 39.8× | 5.77e-5 | 2.00e-3 ✓ sig. |
| germinal center B cell differentiation | GO:0002314 | 2 / 9 | 138× | 8.91e-5 | 2.78e-3 ✓ sig. |
| positive regulation of miRNA transcription | GO:1902895 | 3 / 56 | 33.4× | 9.77e-5 | 2.97e-3 ✓ sig. |
| regulation of G1/S transition of mitotic cell cycle | GO:2000045 | 3 / 57 | 32.8× | 1.03e-4 | 3.09e-3 ✓ sig. |
| fibroblast apoptotic process | GO:0044346 | 2 / 11 | 113× | 1.36e-4 | 3.80e-3 ✓ sig. |
| immune response | GO:0006955 | 6 / 543 | 6.9× | 1.92e-4 | 4.91e-3 ✓ sig. |
| regulation of multicellular organismal development | GO:2000026 | 2 / 15 | 83.1× | 2.58e-4 | 6.05e-3 ✓ sig. |
| positive regulation of developmental process | GO:0051094 | 2 / 16 | 77.9× | 2.95e-4 | 6.63e-3 ✓ sig. |
| natural killer cell differentiation | GO:0001779 | 2 / 19 | 65.6× | 4.19e-4 | 8.50e-3 ✓ sig. |
Pairs within this cluster, by significance
| Disease A ⇵ | Disease B ⇵ | Similarity score ⇵ | Shared genes ⇵ | P-value ⇵ | FDR q-value ⇵ |
|---|---|---|---|---|---|
| Agammaglobulinemia | Burkitt lymphoma | 0.065 | 2 | 1.12e-4 | 3.90e-4 ✓ sig. |
| Agammaglobulinemia | agammaglobulinemia 10, autosomal dominant | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| Agammaglobulinemia | agammaglobulinemia 2, autosomal recessive | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| Agammaglobulinemia | agammaglobulinemia 3, autosomal recessive | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| Agammaglobulinemia | agammaglobulinemia 4, autosomal recessive | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| Agammaglobulinemia | agammaglobulinemia 6, autosomal recessive | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| Agammaglobulinemia | autosomal agammaglobulinemia | 0.071 | 1 | 8.44e-4 | 1.48e-3 ✓ sig. |
| autosomal agammaglobulinemia | Burkitt lymphoma | 0.050 | 1 | 1.23e-3 | 1.97e-3 ✓ sig. |