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Cluster 217

9 diseases · 17 shared-gene connections
9 Diseases
9 Unique genes
0.335 Avg. similarity score
Granulomatous disease Most-connected disease (7 links)
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Disease Searched: Granulomatous disease, chronic, autosomal recessive, 5 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
G6PD 6 / 9 Anemia, congenital, non-spherocytic hemolytic, 1, Anemia, nonspherocytic hemolytic, G6PD deficiency, Granulomatous disease and 2 more
CYBB 2 / 9 Chronic granulomatous disease, x-linked, Granulomatous disease
CYBC1 2 / 9 Granulomatous disease, Granulomatous disease, chronic, autosomal recessive, 5
NCF4 2 / 9 Granulomatous disease, Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type iii
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 ⇵
Cross-presentation of particulate exogenous antigens (phagosomes) Reactome 5 / 8 834× 3.39e-15 8.62e-13 ✓ sig.
RHO GTPases Activate NADPH Oxidases Reactome 5 / 24 278× 2.56e-12 3.75e-10 ✓ sig.
Leishmaniasis KEGG 6 / 78 103× 5.10e-12 7.00e-10 ✓ sig.
ROS and RNS production in phagocytes Reactome 5 / 34 196× 1.67e-11 2.06e-9 ✓ sig.
Detoxification of Reactive Oxygen Species Reactome 5 / 34 196× 1.67e-11 2.06e-9 ✓ sig.
VEGFA-VEGFR2 Pathway Reactome 5 / 62 108× 3.86e-10 3.48e-8 ✓ sig.
Diabetic cardiomyopathy KEGG 6 / 205 39.1× 1.85e-9 1.43e-7 ✓ sig.
Leukocyte transendothelial migration KEGG 5 / 116 57.5× 9.42e-9 6.22e-7 ✓ sig.
Osteoclast differentiation KEGG 5 / 142 47.0× 2.61e-8 1.52e-6 ✓ sig.
Phagocytosis KEGG 5 / 155 43.0× 4.06e-8 2.24e-6 ✓ sig.
Neutrophil extracellular trap formation KEGG 5 / 192 34.8× 1.19e-7 5.79e-6 ✓ sig.
Lipid and atherosclerosis KEGG 5 / 216 30.9× 2.14e-7 9.64e-6 ✓ sig.
Prion disease KEGG 5 / 275 24.3× 7.10e-7 2.75e-5 ✓ sig.
Fluid shear stress and atherosclerosis KEGG 4 / 141 37.9× 2.19e-6 7.27e-5 ✓ sig.
Chemical carcinogenesis - reactive oxygen species KEGG 3 / 227 17.6× 5.15e-4 6.32e-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 ⇵
respiratory burst GO:0045730 5 / 15 692× 1.99e-14 1.20e-11 ✓ sig.
superoxide anion generation GO:0042554 5 / 26 399× 4.35e-13 2.04e-10 ✓ sig.
superoxide metabolic process GO:0006801 4 / 22 378× 1.81e-10 4.81e-8 ✓ sig.
hydrogen peroxide biosynthetic process GO:0050665 3 / 11 566× 1.27e-8 2.03e-6 ✓ sig.
cellular response to L-glutamine GO:1904845 2 / 4 1,038× 1.24e-6 9.54e-5 ✓ sig.
innate immune response GO:0045087 5 / 605 17.2× 3.96e-6 2.45e-4 ✓ sig.
response to aldosterone GO:1904044 2 / 10 415× 9.26e-6 4.78e-4 ✓ sig.
positive regulation of tumor necrosis factor production GO:0032760 3 / 113 55.1× 1.76e-5 7.88e-4 ✓ sig.
reactive oxygen species metabolic process GO:0072593 2 / 45 92.3× 2.02e-4 4.85e-3 ✓ sig.
cellular defense response GO:0006968 2 / 51 81.4× 2.60e-4 5.80e-3 ✓ sig.
positive regulation of phagocytosis GO:0050766 2 / 58 71.6× 3.36e-4 6.94e-3 ✓ sig.
ribose phosphate biosynthetic process GO:0046390 1 / 1 2,076× 4.82e-4 8.81e-3 ✓ sig.
positive regulation of fructose 1,6-bisphosphate metabolic process GO:0060552 1 / 1 2,076× 4.82e-4 8.81e-3 ✓ sig.
negative regulation of glomerular filtration by angiotensin GO:0003106 1 / 1 2,076× 4.82e-4 8.81e-3 ✓ sig.
smooth muscle hypertrophy GO:0014895 1 / 1 2,076× 4.82e-4 8.81e-3 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
G6PD deficiency Hemolytic anemia, g6pd deficient (favism) 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Hemolytic anemia, g6pd deficient (favism) Infections 0.500 1 6.46e-5 1.99e-4 ✓ sig.
G6PD deficiency Infections 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, congenital, non-spherocytic hemolytic, 1 G6PD deficiency 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, nonspherocytic hemolytic Infections 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, nonspherocytic hemolytic Hemolytic anemia, g6pd deficient (favism) 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, nonspherocytic hemolytic G6PD deficiency 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, congenital, non-spherocytic hemolytic, 1 Infections 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, congenital, non-spherocytic hemolytic, 1 Hemolytic anemia, g6pd deficient (favism) 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Anemia, congenital, non-spherocytic hemolytic, 1 Anemia, nonspherocytic hemolytic 0.500 1 6.46e-5 1.99e-4 ✓ sig.
Chronic granulomatous disease, x-linked Granulomatous disease 0.100 1 5.81e-4 1.00e-3 ✓ sig.
G6PD deficiency Granulomatous disease 0.100 1 5.81e-4 1.00e-3 ✓ sig.
Anemia, nonspherocytic hemolytic Granulomatous disease 0.100 1 5.81e-4 1.00e-3 ✓ sig.
Granulomatous disease Hemolytic anemia, g6pd deficient (favism) 0.100 1 5.81e-4 1.00e-3 ✓ sig.
Granulomatous disease Infections 0.100 1 5.81e-4 1.00e-3 ✓ sig.
Granulomatous disease Granulomatous disease, chronic, autosomal recessive, 5 0.100 1 5.81e-4 1.00e-3 ✓ sig.
Granulomatous disease Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type iii 0.100 1 5.81e-4 1.00e-3 ✓ sig.