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Cluster 161

9 diseases · 12 shared-gene connections
9 Diseases
19 Unique genes
0.196 Avg. similarity score
Genetic peripheral neuropathy Most-connected disease (5 links)
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Disease Searched: hereditary peripheral neuropathy 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.

Member diseases (most connected first ‐ the cluster's core)

Top shared genes (genes linked to 2+ member diseases)

Gene ⇵ Member diseases ⇵ Linked diseases
TRPA1 5 / 9 Benign fasciculation-cramp syndrome, Bronchial hyperreactivity, Cramp-fasciculation syndrome, Genetic peripheral neuropathy and 1 more
NGF 3 / 9 Bronchial hyperreactivity, Congenital sensory neuropathy, Overactive bladder
ARHGEF10 2 / 9 autosomal dominant slowed nerve conduction velocity, Genetic peripheral neuropathy
HSPB1 2 / 9 Charcot-Marie-Tooth disease axonal type 2F, Genetic peripheral neuropathy
IGHMBP2 2 / 9 Genetic peripheral neuropathy, hereditary peripheral neuropathy
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 ⇵
Cytokine-cytokine receptor interaction KEGG 7 / 298 14.8× 2.11e-7 1.20e-5 ✓ sig.
Interleukin-10 signaling Reactome 4 / 47 53.8× 7.64e-7 3.69e-5 ✓ sig.
TNF signaling pathway KEGG 4 / 119 21.2× 3.17e-5 8.53e-4 ✓ sig.
Chemokine receptors bind chemokines Reactome 3 / 59 32.1× 1.03e-4 2.25e-3 ✓ sig.
Neuroactive ligand-receptor interaction KEGG 5 / 370 8.5× 2.20e-4 4.10e-3 ✓ sig.
IL-17 signaling pathway KEGG 3 / 94 20.2× 4.11e-4 6.77e-3 ✓ sig.
Rheumatoid arthritis KEGG 3 / 95 20.0× 4.24e-4 6.93e-3 ✓ sig.
Viral protein interaction with cytokine and cytokine receptor KEGG 3 / 100 19.0× 4.93e-4 7.79e-3 ✓ sig.
AGE-RAGE signaling pathway in diabetic complications KEGG 3 / 101 18.8× 5.07e-4 7.96e-3 ✓ sig.
NF-kappa B signaling pathway KEGG 3 / 105 18.1× 5.68e-4 8.70e-3 ✓ sig.
Interleukin-4 and Interleukin-13 signaling Reactome 3 / 108 17.6× 6.17e-4 9.28e-3 ✓ sig.
ADORA2B mediated anti-inflammatory cytokines production Reactome 3 / 128 14.8× 1.01e-3 1.35e-2 ✓ sig.
Glucagon-type ligand receptors Reactome 2 / 33 38.3× 1.22e-3 1.56e-2 ✓ sig.
G alpha (s) signalling events Reactome 3 / 140 13.5× 1.31e-3 1.65e-2 ✓ sig.
Fluid shear stress and atherosclerosis KEGG 3 / 141 13.4× 1.34e-3 1.68e-2 ✓ 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 ⇵
antimicrobial humoral immune response mediated by antimicrobial peptide GO:0061844 6 / 124 47.6× 1.91e-9 3.96e-7 ✓ sig.
sensory perception of pain GO:0019233 4 / 44 89.4× 1.01e-7 1.21e-5 ✓ sig.
inflammatory response GO:0006954 7 / 467 14.7× 2.26e-7 2.40e-5 ✓ sig.
antifungal humoral response GO:0019732 3 / 13 227× 2.53e-7 2.64e-5 ✓ sig.
response to yeast GO:0001878 3 / 16 184× 4.95e-7 4.62e-5 ✓ sig.
immune response GO:0006955 7 / 543 12.7× 6.26e-7 5.63e-5 ✓ sig.
regulation of blood pressure GO:0008217 4 / 83 47.4× 1.33e-6 1.05e-4 ✓ sig.
cell-cell signaling GO:0007267 5 / 234 21.0× 2.97e-6 1.99e-4 ✓ sig.
positive regulation of cytosolic calcium ion concentration GO:0007204 4 / 137 28.7× 9.84e-6 5.19e-4 ✓ sig.
body fluid secretion GO:0007589 2 / 7 281× 2.05e-5 9.21e-4 ✓ sig.
antibacterial humoral response GO:0019731 3 / 65 45.4× 3.74e-5 1.45e-3 ✓ sig.
cellular response to toxic substance GO:0097237 2 / 12 164× 6.43e-5 2.18e-3 ✓ sig.
activation of adenylate cyclase activity GO:0007190 2 / 15 131× 1.02e-4 3.07e-3 ✓ sig.
positive regulation of cAMP/PKA signal transduction GO:0141163 2 / 16 123× 1.17e-4 3.40e-3 ✓ sig.
cellular response to oxygen-containing compound GO:1901701 2 / 16 123× 1.17e-4 3.40e-3 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Bronchial hyperreactivity Overactive bladder 0.118 2 4.60e-6 2.40e-5 ✓ sig.
Benign fasciculation-cramp syndrome Cramp-fasciculation syndrome 0.500 1 6.49e-5 2.33e-4 ✓ sig.
autosomal dominant slowed nerve conduction velocity Genetic peripheral neuropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Benign fasciculation-cramp syndrome Genetic peripheral neuropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Benign fasciculation-cramp syndrome Overactive bladder 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Charcot-Marie-Tooth disease axonal type 2F Genetic peripheral neuropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Congenital sensory neuropathy Overactive bladder 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Cramp-fasciculation syndrome Genetic peripheral neuropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Cramp-fasciculation syndrome Overactive bladder 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Genetic peripheral neuropathy hereditary peripheral neuropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Benign fasciculation-cramp syndrome Bronchial hyperreactivity 0.067 1 9.09e-4 1.58e-3 ✓ sig.
Bronchial hyperreactivity Cramp-fasciculation syndrome 0.067 1 9.09e-4 1.58e-3 ✓ sig.