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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
Diaphyseal bone disorder Peritoneal fibrosis
1 gene
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1 of 1 corroborated by 2+ sources
TGFB1(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Diaphyseal bone disorder inflammatory bowel disease, immunodeficiency, and encephalopathy
1 gene
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1 of 1 corroborated by 2+ sources
TGFB1(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Diastolic heart failure Growth retardation, developmental delay, and facial dysmorphism
1 gene
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1 of 1 corroborated by 2+ sources
FTO(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Diastolic heart failure Growth retardation, developmental delay, coarse facies, and early death
1 gene
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1 of 1 corroborated by 2+ sources
FTO(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Dicer1 syndrome Granulosa cell tumor of ovary
1 gene
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1 of 1 corroborated by 2+ sources
DICER1(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 395 →
Dicer1 syndrome Vertebral anomalies with endocrine and t-cell dysfunction
1 gene
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1 of 1 corroborated by 2+ sources
DICER1(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 395 →
Diffuse nonepidermolytic palmoplantar keratoderma Epidermolytic ichthyosis
1 gene
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1 of 1 corroborated by 2+ sources
KRT1(5)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 230 →
Diffuse palmoplantar keratoderma Focal palmoplantar keratoderma with joint keratoses
1 gene
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1 of 1 corroborated by 2+ sources
DSG1(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Digital clubbing, isolated congenital Medullary carcinoma
1 gene
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1 of 1 corroborated by 2+ sources
HPGD(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Digital clubbing, isolated congenital Primary hypertrophic osteoarthropathy
1 gene
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1 of 1 corroborated by 2+ sources
HPGD(5)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Dihydrolipoamide dehydrogenase deficiency pyruvate dehydrogenase E3 deficiency
1 gene
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1 of 1 corroborated by 2+ sources
DLD(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Dihydropyrimidinase deficiency Dihydropyrimidine metabolism disorder
1 gene
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1 of 1 corroborated by 2+ sources
DPYS(5)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 349 →
Dihydropyrimidine dehydrogenase deficiency Dihydropyrimidine metabolism disorder
1 gene
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1 of 1 corroborated by 2+ sources
DPYD(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 349 →
Dilatation of pulmonary artery Right bundle branch block
1 gene
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BMPR2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Dilatation of pulmonary artery Right cardiac ventricular dilatation
1 gene
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BMPR2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
dilated cardiomyopathy 1A Restrictive dermopathy
1 gene
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1 of 1 corroborated by 2+ sources
LMNA(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 65 →
dilated cardiomyopathy 1E Ectopic rhythm
1 gene
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1 of 1 corroborated by 2+ sources
SCN5A(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 129 →
dilated cardiomyopathy 1E Paroxysmal ventricular fibrillation
1 gene
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1 of 1 corroborated by 2+ sources
SCN5A(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 129 →
dilated cardiomyopathy 1EE Keppen-lubinsky syndrome
1 gene
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1 of 1 corroborated by 2+ sources
MYH6(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 318 →
dilated cardiomyopathy 1S Ebstein anomaly
1 gene
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1 of 1 corroborated by 2+ sources
MYH7(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 89 →
dilated cardiomyopathy 1S Parieto-occipital craniosynostosis
1 gene
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1 of 1 corroborated by 2+ sources
MYH7(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 89 →
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Restrictive dermopathy
1 gene
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1 of 1 corroborated by 2+ sources
LMNA(5)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 65 →
Distal amyotrophy Distal myotilinopathy
1 gene
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1 of 1 corroborated by 2+ sources
MYOT(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Dkc1-related disorder X-linked dyskeratosis congenita
1 gene
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1 of 1 corroborated by 2+ sources
DKC1(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 64 →
Dna ligase iv deficiency Dubowitz syndrome
1 gene
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1 of 1 corroborated by 2+ sources
LIG4(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —

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