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 28
19
Diseases
50
Unique genes
0.198
Avg. similarity score
Epidermal nevus
Most-connected disease (12 links)
Disease
Searched: Hypophosphatemic rickets
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Hypophosphatemic rickets
Epidermal nevus
Schimmelpenning-feuerstein-mims syndrome
Penile neoplasms
Autoimmune lymphoproliferative disorder
Bladder cancer
Splenic neoplasms
Nonmedullary thyroid cancer
Woolly hair nevus
Congenital arteriovenous malformation
Follicular thyroid cancer
Melanocytic nevus
Neurofibrosarcoma
Seminoma
ciliary dyskinesia, primary, 39
autoimmune lymphoproliferative syndrome type 2A
bamforth-lazarus syndrome
immunodeficiency 64
lymphoproliferative syndrome 1
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Epidermal nevus | 12 | 12 | 7 |
| Schimmelpenning-feuerstein-mims syndrome | 10 | 10 | 3 |
| Penile neoplasms | 7 | 7 | 4 |
| Autoimmune lymphoproliferative disorder | 6 | 6 | 11 |
| Bladder cancer | 6 | 6 | 4 |
| Splenic neoplasms | 6 | 6 | 1 |
| Nonmedullary thyroid cancer | 5 | 5 | 7 |
| Woolly hair nevus | 5 | 5 | 1 |
| Congenital arteriovenous malformation | 4 | 4 | 9 |
| Follicular thyroid cancer | 4 | 4 | 7 |
| Hypophosphatemic rickets | 4 | 4 | 12 |
| Melanocytic nevus | 4 | 4 | 11 |
| Neurofibrosarcoma | 4 | 4 | 1 |
| Seminoma | 4 | 4 | 3 |
| ciliary dyskinesia, primary, 39 | 3 | 3 | 1 |
| autoimmune lymphoproliferative syndrome type 2A | 1 | 1 | 1 |
| bamforth-lazarus syndrome | 1 | 1 | 1 |
| immunodeficiency 64 | 1 | 1 | 1 |
| lymphoproliferative syndrome 1 | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| HRAS | 12 / 19 | Bladder cancer, Congenital arteriovenous malformation, Epidermal nevus, Follicular thyroid cancer and 8 more |
| NRAS | 7 / 19 | Autoimmune lymphoproliferative disorder, Epidermal nevus, Follicular thyroid cancer, Melanocytic nevus and 3 more |
| KRAS | 5 / 19 | Autoimmune lymphoproliferative disorder, Bladder cancer, Epidermal nevus, Penile neoplasms and 1 more |
| LRRC56 | 4 / 19 | ciliary dyskinesia, primary, 39, Congenital arteriovenous malformation, Epidermal nevus, Hypophosphatemic rickets |
| FGFR3 | 3 / 19 | Bladder cancer, Epidermal nevus, Seminoma |
| PIK3CA | 3 / 19 | Congenital arteriovenous malformation, Epidermal nevus, Penile neoplasms |
| CASP10 | 2 / 19 | Autoimmune lymphoproliferative disorder, autoimmune lymphoproliferative syndrome type 2A |
| CASP8 | 2 / 19 | Autoimmune lymphoproliferative disorder, Melanocytic nevus |
| FOXE1 | 2 / 19 | bamforth-lazarus syndrome, Nonmedullary thyroid cancer |
| ITK | 2 / 19 | Autoimmune lymphoproliferative disorder, lymphoproliferative syndrome 1 |
| MINPP1 | 2 / 19 | Follicular thyroid cancer, Nonmedullary thyroid cancer |
| RASGRP1 | 2 / 19 | Autoimmune lymphoproliferative disorder, immunodeficiency 64 |
| SRGAP1 | 2 / 19 | Follicular thyroid cancer, Nonmedullary thyroid cancer |
| TP53 | 2 / 19 | Melanocytic nevus, Penile 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 ⇵ |
|---|---|---|---|---|---|
| Apoptosis | KEGG | 11 / 137 | 19.3× | 7.25e-12 | 1.28e-9 ✓ sig. |
| Hepatitis B | KEGG | 11 / 163 | 16.2× | 4.85e-11 | 7.05e-9 ✓ sig. |
| Thyroid cancer | KEGG | 7 / 37 | 45.4× | 1.31e-10 | 1.75e-8 ✓ sig. |
| Pathways in cancer | KEGG | 16 / 533 | 7.2× | 2.20e-10 | 2.76e-8 ✓ sig. |
| Signaling by FGFR3 fusions in cancer | Reactome | 5 / 10 | 120× | 2.53e-10 | 3.13e-8 ✓ sig. |
| Signaling by FGFR3 point mutants in cancer | Reactome | 6 / 22 | 65.5× | 2.71e-10 | 3.33e-8 ✓ sig. |
| Bladder cancer | KEGG | 7 / 41 | 41.0× | 2.83e-10 | 3.46e-8 ✓ sig. |
| Melanoma | KEGG | 8 / 73 | 26.3× | 5.50e-10 | 6.27e-8 ✓ sig. |
| Hepatitis C | KEGG | 10 / 159 | 15.1× | 8.11e-10 | 8.88e-8 ✓ sig. |
| Activation of RAS in B cells | Reactome | 4 / 5 | 192× | 1.32e-9 | 1.36e-7 ✓ sig. |
| FasL/ CD95L signaling | Reactome | 4 / 5 | 192× | 1.32e-9 | 1.36e-7 ✓ sig. |
| MAPK signaling pathway | KEGG | 12 / 299 | 9.6× | 2.37e-9 | 2.33e-7 ✓ sig. |
| Ras signaling pathway | KEGG | 11 / 237 | 11.1× | 2.66e-9 | 2.60e-7 ✓ sig. |
| GnRH secretion | KEGG | 7 / 65 | 25.9× | 8.12e-9 | 7.05e-7 ✓ sig. |
| SHC-mediated cascade:FGFR3 | Reactome | 5 / 18 | 66.7× | 8.38e-9 | 7.22e-7 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| intracellular phosphate ion homeostasis | GO:0030643 | 4 / 10 | 149× | 9.41e-9 | 1.58e-6 ✓ sig. |
| thyroid gland development | GO:0030878 | 5 / 30 | 62.3× | 1.51e-8 | 2.42e-6 ✓ sig. |
| Ras protein signal transduction | GO:0007265 | 6 / 79 | 28.4× | 6.45e-8 | 8.40e-6 ✓ sig. |
| cellular senescence | GO:0090398 | 5 / 57 | 32.8× | 4.21e-7 | 4.09e-5 ✓ sig. |
| positive regulation of neuron apoptotic process | GO:0043525 | 5 / 65 | 28.7× | 8.17e-7 | 7.10e-5 ✓ sig. |
| biomineral tissue development | GO:0031214 | 4 / 35 | 42.7× | 2.23e-6 | 1.60e-4 ✓ sig. |
| MAPK cascade | GO:0000165 | 6 / 147 | 15.3× | 2.56e-6 | 1.79e-4 ✓ sig. |
| cellular response to parathyroid hormone stimulus | GO:0071374 | 3 / 11 | 102× | 2.93e-6 | 2.00e-4 ✓ sig. |
| response to magnesium ion | GO:0032026 | 3 / 12 | 93.4× | 3.90e-6 | 2.51e-4 ✓ sig. |
| neuron apoptotic process | GO:0051402 | 5 / 98 | 19.1× | 6.29e-6 | 3.68e-4 ✓ sig. |
| positive regulation of gene expression | GO:0010628 | 9 / 504 | 6.7× | 6.58e-6 | 3.81e-4 ✓ sig. |
| animal organ development | GO:0048513 | 5 / 102 | 18.3× | 7.65e-6 | 4.31e-4 ✓ sig. |
| phosphate ion homeostasis | GO:0055062 | 3 / 15 | 74.7× | 8.02e-6 | 4.48e-4 ✓ sig. |
| thymus development | GO:0048538 | 4 / 50 | 29.9× | 9.54e-6 | 5.13e-4 ✓ sig. |
| glial cell proliferation | GO:0014009 | 3 / 18 | 62.3× | 1.43e-5 | 7.02e-4 ✓ sig. |