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 18
21
Diseases
162
Unique genes
0.197
Avg. similarity score
Adrenocortical carcinoma
Most-connected disease (11 links)
Disease
Searched: Adrenocortical carcinoma
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Adrenocortical carcinoma
Choroid plexus carcinoma
Choroid plexus papilloma
B-lymphoblastic leukemia/lymphoma
Urogenital neoplasms
Vulvar lichen sclerosus
Urologic neoplasms
B-cell chronic lymphocytic leukemia
Demyelinating diseases
Li-fraumeni syndrome
Sapho syndrome
B-cell acute lymphoblastic leukemia
Central nervous system neoplasms
Chromosome 17 deletion
Small cell carcinoma
Lymphoblastic leukemia
Familial telangiectasia cancer syndrome
Merkel cell carcinoma
Uinary system neoplasms
granulocytopenia with immunoglobulin abnormality
leukemia, acute myeloid, susceptibility to
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Adrenocortical carcinoma | 11 | 11 | 1 |
| Choroid plexus carcinoma | 11 | 11 | 1 |
| Choroid plexus papilloma | 10 | 10 | 1 |
| B-lymphoblastic leukemia/lymphoma | 6 | 6 | 19 |
| Urogenital neoplasms | 6 | 6 | 5 |
| Vulvar lichen sclerosus | 6 | 6 | 2 |
| Urologic neoplasms | 5 | 5 | 8 |
| B-cell chronic lymphocytic leukemia | 4 | 4 | 8 |
| Demyelinating diseases | 4 | 4 | 11 |
| Li-fraumeni syndrome | 4 | 4 | 5 |
| Sapho syndrome | 4 | 4 | 5 |
| B-cell acute lymphoblastic leukemia | 3 | 3 | 60 |
| Central nervous system neoplasms | 3 | 3 | 2 |
| Chromosome 17 deletion | 3 | 3 | 2 |
| Small cell carcinoma | 3 | 3 | 9 |
| Lymphoblastic leukemia | 2 | 2 | 57 |
| Familial telangiectasia cancer syndrome | 1 | 1 | 1 |
| Merkel cell carcinoma | 1 | 1 | 1 |
| Uinary system neoplasms | 1 | 1 | 2 |
| granulocytopenia with immunoglobulin abnormality | 1 | 1 | 1 |
| leukemia, acute myeloid, susceptibility to | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| TP53 | 14 / 21 | Adrenocortical carcinoma, B-cell chronic lymphocytic leukemia, B-lymphoblastic leukemia/lymphoma, Central nervous system neoplasms and 10 more |
| CDKN2A | 5 / 21 | B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Li-fraumeni syndrome, Urogenital neoplasms and 1 more |
| FLT3 | 4 / 21 | B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, leukemia, acute myeloid, susceptibility to, Lymphoblastic leukemia |
| IKZF1 | 3 / 21 | B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Lymphoblastic leukemia |
| PIP4K2A | 3 / 21 | B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Lymphoblastic leukemia |
| ARID5B | 2 / 21 | B-cell acute lymphoblastic leukemia, Lymphoblastic leukemia |
| ATR | 2 / 21 | Familial telangiectasia cancer syndrome, Urologic neoplasms |
| BCR | 2 / 21 | B-lymphoblastic leukemia/lymphoma, Lymphoblastic leukemia |
| CCND1 | 2 / 21 | B-cell chronic lymphocytic leukemia, Urologic neoplasms |
| CEBPE | 2 / 21 | B-cell acute lymphoblastic leukemia, Lymphoblastic leukemia |
| GATA3 | 2 / 21 | B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma |
| GSDMB | 2 / 21 | B-cell acute lymphoblastic leukemia, Lymphoblastic leukemia |
| HYOU1 | 2 / 21 | B-cell acute lymphoblastic leukemia, granulocytopenia with immunoglobulin abnormality |
| IKZF3 | 2 / 21 | B-cell acute lymphoblastic leukemia, B-cell chronic lymphocytic leukemia |
| LHPP | 2 / 21 | B-cell acute lymphoblastic leukemia, Lymphoblastic leukemia |
| MDM2 | 2 / 21 | Li-fraumeni syndrome, Sapho syndrome |
| MYC | 2 / 21 | Demyelinating diseases, Merkel cell carcinoma |
| PAX5 | 2 / 21 | B-lymphoblastic leukemia/lymphoma, Lymphoblastic leukemia |
| SLC2A13 | 2 / 21 | Uinary system neoplasms, Urogenital neoplasms |
| SULT1A1 | 2 / 21 | B-cell acute lymphoblastic leukemia, Urologic neoplasms |
| WDR11 | 2 / 21 | Uinary system neoplasms, Urogenital 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 ⇵ |
|---|---|---|---|---|---|
| Transcriptional misregulation in cancer | KEGG | 18 / 198 | 6.7× | 1.62e-10 | 2.11e-8 ✓ sig. |
| Cellular senescence | KEGG | 16 / 157 | 7.6× | 3.27e-10 | 3.96e-8 ✓ sig. |
| Chronic myeloid leukemia | KEGG | 11 / 77 | 10.6× | 5.93e-9 | 5.34e-7 ✓ sig. |
| Human cytomegalovirus infection | KEGG | 16 / 226 | 5.2× | 6.39e-8 | 4.43e-6 ✓ sig. |
| Glioma | KEGG | 10 / 76 | 9.8× | 6.70e-8 | 4.61e-6 ✓ sig. |
| Stabilization of p53 | Reactome | 5 / 11 | 33.7× | 1.82e-7 | 1.10e-5 ✓ sig. |
| Pathways in cancer | KEGG | 24 / 533 | 3.3× | 1.89e-7 | 1.14e-5 ✓ sig. |
| Human T-cell leukemia virus 1 infection | KEGG | 15 / 224 | 5.0× | 3.47e-7 | 1.95e-5 ✓ sig. |
| Melanoma | KEGG | 9 / 73 | 9.1× | 5.49e-7 | 2.90e-5 ✓ sig. |
| p53 signaling pathway | KEGG | 9 / 75 | 8.9× | 6.94e-7 | 3.54e-5 ✓ sig. |
| Pancreatic cancer | KEGG | 9 / 77 | 8.7× | 8.71e-7 | 4.31e-5 ✓ sig. |
| Bladder cancer | KEGG | 7 / 41 | 12.7× | 1.09e-6 | 5.25e-5 ✓ sig. |
| Kaposi sarcoma-associated herpesvirus infection | KEGG | 13 / 196 | 4.9× | 2.42e-6 | 1.05e-4 ✓ sig. |
| Acute myeloid leukemia | KEGG | 8 / 68 | 8.7× | 3.43e-6 | 1.41e-4 ✓ sig. |
| Small cell lung cancer | KEGG | 9 / 93 | 7.2× | 4.32e-6 | 1.72e-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 ⇵ |
|---|---|---|---|---|---|
| positive regulation of transcription by RNA polymerase II | GO:0045944 | 37 / 1,208 | 3.5× | 1.03e-11 | 3.75e-9 ✓ sig. |
| regulation of cell cycle | GO:0051726 | 15 / 262 | 6.6× | 9.25e-9 | 1.56e-6 ✓ sig. |
| intrinsic apoptotic signaling pathway in response to DNA damage | GO:0008630 | 8 / 54 | 17.1× | 1.99e-8 | 3.07e-6 ✓ sig. |
| positive regulation of gene expression | GO:0010628 | 19 / 504 | 4.3× | 8.14e-8 | 1.03e-5 ✓ sig. |
| response to gamma radiation | GO:0010332 | 6 / 27 | 25.6× | 9.85e-8 | 1.20e-5 ✓ sig. |
| negative regulation of DNA-templated transcription | GO:0045892 | 21 / 631 | 3.8× | 1.33e-7 | 1.56e-5 ✓ sig. |
| replicative senescence | GO:0090399 | 5 / 16 | 36.0× | 1.86e-7 | 2.07e-5 ✓ sig. |
| regulation of cellular response to stress | GO:0080135 | 5 / 18 | 32.0× | 3.60e-7 | 3.57e-5 ✓ sig. |
| embryonic hemopoiesis | GO:0035162 | 5 / 18 | 32.0× | 3.60e-7 | 3.57e-5 ✓ sig. |
| cell population proliferation | GO:0008283 | 13 / 263 | 5.7× | 5.09e-7 | 4.81e-5 ✓ sig. |
| post-embryonic development | GO:0009791 | 8 / 82 | 11.3× | 5.55e-7 | 5.16e-5 ✓ sig. |
| macrophage differentiation | GO:0030225 | 6 / 37 | 18.7× | 7.20e-7 | 6.41e-5 ✓ sig. |
| regulation of cell population proliferation | GO:0042127 | 11 / 201 | 6.3× | 1.47e-6 | 1.15e-4 ✓ sig. |
| cellular response to xenobiotic stimulus | GO:0071466 | 7 / 65 | 12.4× | 1.48e-6 | 1.15e-4 ✓ sig. |
| spleen development | GO:0048536 | 6 / 42 | 16.5× | 1.57e-6 | 1.20e-4 ✓ sig. |