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 147
9
Diseases
81
Unique genes
0.056
Avg. similarity score
Gallbladder neoplasms
Most-connected disease (5 links)
Disease
Searched: Primary aldosteronism
Pinned (dragged)
Node size = connections within this cluster · edge thickness = similarity strength · hover an edge for its details ·
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Primary aldosteronism
Gallbladder neoplasms
Peters plus syndrome
Potassium deficiency
Disorder of sex development
Hyperplasia
Conjunctival disease
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
neuropathy, hereditary sensory, type 1D
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Gallbladder neoplasms | 5 | 5 | 25 |
| Primary aldosteronism | 5 | 5 | 16 |
| Peters plus syndrome | 4 | 4 | 1 |
| Potassium deficiency | 4 | 4 | 18 |
| Disorder of sex development | 3 | 3 | 1 |
| Hyperplasia | 2 | 2 | 31 |
| Conjunctival disease | 1 | 1 | 2 |
| Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome | 1 | 1 | 1 |
| neuropathy, hereditary sensory, type 1D | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| B3GLCT | 5 / 9 | Gallbladder neoplasms, Hyperplasia, Peters plus syndrome, Potassium deficiency and 1 more |
| RXFP2 | 5 / 9 | Disorder of sex development, Gallbladder neoplasms, Hyperplasia, Potassium deficiency and 1 more |
| ATL1 | 2 / 9 | neuropathy, hereditary sensory, type 1D, Potassium deficiency |
| CASZ1 | 2 / 9 | Potassium deficiency, Primary aldosteronism |
| CCKAR | 2 / 9 | Gallbladder neoplasms, Primary aldosteronism |
| DAPK1 | 2 / 9 | Conjunctival disease, Gallbladder neoplasms |
| LSP1 | 2 / 9 | Potassium deficiency, Primary aldosteronism |
| NDP | 2 / 9 | Hyperplasia, Primary aldosteronism |
| UCHL1 | 2 / 9 | Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome, Gallbladder neoplasms |
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 ⇵ |
|---|---|---|---|---|---|
| Pathways in cancer | KEGG | 23 / 533 | 6.4× | 4.13e-13 | 8.96e-11 ✓ sig. |
| Gastric cancer | KEGG | 14 / 150 | 13.8× | 1.08e-12 | 2.19e-10 ✓ sig. |
| Prostate cancer | KEGG | 12 / 98 | 18.2× | 1.94e-12 | 3.75e-10 ✓ sig. |
| Colorectal cancer | KEGG | 11 / 87 | 18.7× | 1.21e-11 | 2.03e-9 ✓ sig. |
| Hepatocellular carcinoma | KEGG | 13 / 170 | 11.3× | 9.41e-11 | 1.30e-8 ✓ sig. |
| Interleukin-4 and Interleukin-13 signaling | Reactome | 11 / 108 | 15.1× | 1.33e-10 | 1.77e-8 ✓ sig. |
| Endometrial cancer | KEGG | 9 / 59 | 22.6× | 1.75e-10 | 2.27e-8 ✓ sig. |
| Proteoglycans in cancer | KEGG | 13 / 204 | 9.4× | 9.10e-10 | 9.83e-8 ✓ sig. |
| Breast cancer | KEGG | 11 / 148 | 11.0× | 3.97e-9 | 3.74e-7 ✓ sig. |
| Bladder cancer | KEGG | 7 / 41 | 25.3× | 9.11e-9 | 7.79e-7 ✓ sig. |
| Signaling by ERBB2 KD Mutants | Reactome | 6 / 25 | 35.6× | 1.25e-8 | 1.03e-6 ✓ sig. |
| Endocrine resistance | KEGG | 9 / 99 | 13.5× | 1.94e-8 | 1.53e-6 ✓ sig. |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | Reactome | 9 / 103 | 13.0× | 2.75e-8 | 2.08e-6 ✓ sig. |
| Pancreatic cancer | KEGG | 8 / 77 | 15.4× | 4.35e-8 | 3.12e-6 ✓ sig. |
| PI3K events in ERBB2 signaling | Reactome | 5 / 16 | 46.3× | 5.08e-8 | 3.59e-6 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| negative regulation of apoptotic process | GO:0043066 | 16 / 524 | 7.0× | 7.28e-10 | 1.63e-7 ✓ sig. |
| positive regulation of miRNA transcription | GO:1902895 | 7 / 56 | 28.8× | 4.31e-9 | 7.97e-7 ✓ sig. |
| positive regulation of epithelial cell proliferation | GO:0050679 | 7 / 73 | 22.1× | 2.86e-8 | 4.20e-6 ✓ sig. |
| positive regulation of gene expression | GO:0010628 | 14 / 504 | 6.4× | 3.14e-8 | 4.54e-6 ✓ sig. |
| positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | GO:0051897 | 10 / 217 | 10.6× | 3.32e-8 | 4.76e-6 ✓ sig. |
| glucose homeostasis | GO:0042593 | 8 / 134 | 13.8× | 1.17e-7 | 1.40e-5 ✓ sig. |
| positive regulation of transcription by RNA polymerase II | GO:0045944 | 20 / 1,208 | 3.8× | 1.47e-7 | 1.70e-5 ✓ sig. |
| cellular response to hypoxia | GO:0071456 | 8 / 139 | 13.3× | 1.56e-7 | 1.78e-5 ✓ sig. |
| cell population proliferation | GO:0008283 | 10 / 263 | 8.8× | 2.01e-7 | 2.21e-5 ✓ sig. |
| neuron apoptotic process | GO:0051402 | 7 / 98 | 16.5× | 2.22e-7 | 2.41e-5 ✓ sig. |
| response to oxidative stress | GO:0006979 | 8 / 146 | 12.6× | 2.28e-7 | 2.46e-5 ✓ sig. |
| response to UV-A | GO:0070141 | 3 / 4 | 173× | 3.13e-7 | 3.19e-5 ✓ sig. |
| epidermal growth factor receptor signaling pathway | GO:0007173 | 6 / 64 | 21.6× | 3.37e-7 | 3.39e-5 ✓ sig. |
| positive regulation of MAPK cascade | GO:0043410 | 9 / 224 | 9.3× | 5.37e-7 | 5.02e-5 ✓ sig. |
| negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway | GO:1902176 | 4 / 18 | 51.3× | 9.57e-7 | 8.06e-5 ✓ sig. |