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What do these columns mean?
Shared genes
Curated genes linked to both diseases (disease_gdp). The line below it shows how many of those are "corroborated" -- backed by 2+ independent database sources combined across both diseases, not resting on a single source's say-so.
Similarity score
Jaccard-based: shared genes ÷ the union of both diseases' entire gene sets, with a small boost from users who bookmarked both diseases. Treats both diseases symmetrically.
Overlap coefficient
Shared genes ÷ the smaller disease's own total gene count. Complements the similarity score above for asymmetric pairs -- e.g. a rare disease almost entirely "contained" in a common disease's much larger gene set scores low on Jaccard but high here.
P-value / FDR q-value
Is this gene overlap more than chance? An upper-tail hypergeometric test, Benjamini-Hochberg corrected across every tested pair (the q-value is the one that accounts for testing thousands of pairs at once -- prefer it over the raw p-value).
Shared cluster
Links to a multi-disease cluster (see Disease Clusters) if both diseases of this pair were independently grouped together by that separate analysis.
ⓘ Shows only pairs whose gene overlap is too large to be down to chance (FDR q-value below 0.05). These are the rows marked ✓ sig. in the table. ⓘ Shows only pairs where both diseases also belong to the same group on the Disease Clusters page. Two separate analyses agree they're related, so the link is stronger. These are the rows with a link in the Shared cluster column.
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Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▲ Shared cluster
Brain cancer Small cell lung carcinoma
2 genes
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FCHO2(1), FOXN3(1)
0.021 0.400 3.41e-4 8.10e-4 ✓ sig. —
Hyperaldosteronism Sick sinus syndrome
2 genes
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2 of 2 corroborated by 2+ sources
CACNA1D(2), KCNJ5(6)
0.049 0.111 3.51e-4 8.32e-4 ✓ sig. —
Hyperaldosteronism Potassium deficiency
2 genes
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B3GLCT(1), RXFP2(1)
0.049 0.111 3.51e-4 8.32e-4 ✓ sig. —
Pharyngeal disorder Rosacea
2 genes
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IKZF1(1), SPMIP7(1)
0.045 0.143 3.52e-4 8.34e-4 ✓ sig. —
Bell's palsy Facial nerve disorder
2 genes
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CDC5L(1), SUPT3H(1)
0.032 0.250 3.59e-4 8.50e-4 ✓ sig. —
Clonal hematopoiesis Ileocolitis
2 genes
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LY75(1), LY75-CD302(1)
0.032 0.250 3.59e-4 8.50e-4 ✓ sig. —
Congenital diaphragmatic hernia Syndactyly
2 genes
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GLI3(1), FREM2(1)
0.049 0.100 3.65e-4 8.64e-4 ✓ sig. —
Colonic polyps Thoracic disease
1 gene
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1 of 1 corroborated by 2+ sources
ILK(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Combined deficiency of factor v and factor viii Combined immunodeficiency, enteropathy spectrum
1 gene
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1 of 1 corroborated by 2+ sources
MCFD2(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Combined deficiency of factor v and factor viii Gastrointestinal defects and immunodeficiency syndrome
1 gene
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1 of 1 corroborated by 2+ sources
MCFD2(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Combined factor v and factor viii deficiency Combined immunodeficiency, enteropathy spectrum
1 gene
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1 of 1 corroborated by 2+ sources
MCFD2(6)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Combined factor v and factor viii deficiency Gastrointestinal defects and immunodeficiency syndrome
1 gene
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1 of 1 corroborated by 2+ sources
MCFD2(6)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Activated pi3k-delta syndrome Combined immunodeficiency with facio-oculo-skeletal anomalies
1 gene
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1 of 1 corroborated by 2+ sources
PIK3CD(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 181 →
Combined immunodeficiency with granulomatosis Salla disease
1 gene
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1 of 1 corroborated by 2+ sources
RAG2(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 173 →
Combined immunodeficiency-multiple intestinal atresia Heparin cofactor 2 deficiency
1 gene
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1 of 1 corroborated by 2+ sources
PI4KA(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 267 →
Congenital bone marrow failure syndrome Growth hormone insensitivity syndrome with immune dysregulation
1 gene
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1 of 1 corroborated by 2+ sources
ERCC6L2(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 3 →
Congenital cardiomyopathy Myoclonic epilepsy with ragged red fibers
1 gene
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ND5(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 32 →
Congenital facial anomaly Hypoplastic anemia
1 gene
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1 of 1 corroborated by 2+ sources
CAD(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 168 →
Congenital facial anomaly Congenital hypoplastic anemia
1 gene
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CAD(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 168 →
Congenital hemangioma Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
1 gene
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1 of 1 corroborated by 2+ sources
GNA11(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 40 →
Congenital kidney anomaly Polycystic kidney disease with tuberous sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
PKD1(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 70 →
Congenital kidney anomaly Renovascular hypertension
1 gene
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PKD1(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 70 →
Congenital kidney anomaly Pancreatic cyst
1 gene
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PKD1(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 70 →
Congenital leukocyte adherence deficiency Leukocyte disorders
1 gene
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1 of 1 corroborated by 2+ sources
ITGB2(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 155 →
Intellectual developmental disorder autism speech Intellectual developmental disorder speech autism dysmorphic
1 gene
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1 of 1 corroborated by 2+ sources
TBR1(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 275 →

Showing 25 of 20813 pairs, sorted by significance (ascending). Click a column header to sort.