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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
Huntington disease Hypotension
5 genes
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5 of 5 corroborated by 2+ sources
GRIN2B(2), MAOA(2), MAOB(2), IL6(2), CNR1(2)
0.040 0.082 6.60e-6 3.35e-5 ✓ sig. —
Heart valve prolapse Oral submucous fibrosis
3 genes
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3 of 3 corroborated by 2+ sources
COL1A1(2), TIMP1(2), COL1A2(2)
0.064 0.150 6.70e-6 3.40e-5 ✓ sig. —
Hodgkin disease Hyper-immunoglobulin m syndrome
2 genes
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2 of 2 corroborated by 2+ sources
CD40LG(2), CD40(2)
0.100 0.500 6.87e-6 3.49e-5 ✓ sig. Cluster 131 →
Bronchiectasis Extrinsic allergic alveolitis
2 genes
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1 of 2 corroborated by 2+ sources
TNF(2), TAP1(1)
0.100 0.500 6.87e-6 3.49e-5 ✓ sig. —
Congenital fusion of ribs Micrognathism
2 genes
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0.100 0.500 6.87e-6 3.49e-5 ✓ sig. —
Cervical intraepithelial neoplasia Gastroparesis
2 genes
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0.125 0.333 6.95e-6 3.52e-5 ✓ sig. Cluster 1 →
Infantile spasms Tuberous sclerosis complex
2 genes
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2 of 2 corroborated by 2+ sources
TSC2(7), TSC1(7)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. —
Ovarian mucinous adenocarcinoma Testicular hydrocele
2 genes
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INHBB(1), PAX8(1)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. —
Cardiovascular abnormalities Vascular remodeling
2 genes
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2 of 2 corroborated by 2+ sources
GATA2(2), AGT(2)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. Cluster 136 →
Arthrogryposis Digitotalar dysmorphism
2 genes
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1 of 2 corroborated by 2+ sources
MYH3(1), TPM2(2)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. Cluster 202 →
Cushing's disease Penile disease
2 genes
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2 of 2 corroborated by 2+ sources
ATRX(2), POMC(2)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. —
Ductal carcinoma Lobular carcinoma
2 genes
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CDH1(1), STAT5A(1)
0.125 0.333 6.95e-6 3.52e-5 ✓ sig. —
Meningioma Schwannomatosis
2 genes
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2 of 2 corroborated by 2+ sources
SMARCB1(4), NF2(5)
0.077 0.667 6.98e-6 3.53e-5 ✓ sig. —
Blood coagulation disorder Combined deficiency of vitamin k-dependent clotting factors
2 genes
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2 of 2 corroborated by 2+ sources
VKORC1(5), GGCX(6)
0.077 0.667 6.98e-6 3.53e-5 ✓ sig. —
Mitochondrial hepatopathy Polyneuropathy
2 genes
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POLG(1), POLGARF(1)
0.077 0.667 6.98e-6 3.53e-5 ✓ sig. —
Becker muscular dystrophy Conduction disorder of the heart
2 genes
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1 of 2 corroborated by 2+ sources
DMD(4), PKP2(1)
0.077 0.667 6.98e-6 3.53e-5 ✓ sig. —
Hemorrhage Warfarin sensitivity
2 genes
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NQO1(1), CYP2C9(1)
0.077 0.667 6.98e-6 3.53e-5 ✓ sig. —
Essential thrombocythemia Myelodysplastic syndrome
3 genes
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3 of 3 corroborated by 2+ sources
TP53(3), TET2(5), JAK2(4)
0.053 0.231 6.99e-6 3.53e-5 ✓ sig. Cluster 53 →
Hemangiosarcoma Temporal lobe epilepsy
3 genes
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3 of 3 corroborated by 2+ sources
VEGFA(2), TEK(2), KDR(2)
0.061 0.167 7.16e-6 3.62e-5 ✓ sig. —
Diabetic ketoacidosis Neonatal diabetes mellitus
3 genes
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3 of 3 corroborated by 2+ sources
INS(3), INS-IGF2(2), SLC2A2(3)
0.060 0.176 7.16e-6 3.62e-5 ✓ sig. Cluster 36 →
Benign prostatic hyperplasia Toxic nodular goiter
3 genes
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TERT(1), SLK(1), STN1(1)
0.060 0.176 7.16e-6 3.62e-5 ✓ sig. —
Bipolar depression Non-organic psychosis
6 genes
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ANK3(1), GCH1(1), CACNA1C(1), TENM4(1), TRPM2(1), GRIK4(1)
0.036 0.087 7.37e-6 3.72e-5 ✓ sig. —
Atherosclerosis Erectile dysfunction
6 genes
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5 of 6 corroborated by 2+ sources
CELA2A(3), VEGFA(2), NOS3(2), EDN1(2), EDNRA(3), TDRD15(1)
0.034 0.098 7.37e-6 3.72e-5 ✓ sig. —
Esophageal adenocarcinoma Peptic ulcer disease
5 genes
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BCL3(1), FOXP1(1), BARX1(1), SLC22A3(1), TPPP(1)
0.033 0.143 7.41e-6 3.74e-5 ✓ sig. —
Congenital nasopharyngeal atresia Situs inversus
3 genes
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DNAH5(1), DNAH11(1), DNAAF19(1)
0.063 0.150 7.44e-6 3.75e-5 ✓ sig. —

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