Shared-Gene Disease Pairs?

Disease pairs ranked by curated gene overlap — a data-driven way to spot diseases that aren't normally considered related but share a large number of underlying genes. Looking for groups of more than two? See Disease Clusters.

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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
Abri amyloidosis Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(2)
0.500 1.000 6.46e-5 1.98e-4 ✓ sig. —
Familial danish dementia Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(2)
0.500 1.000 6.46e-5 1.98e-4 ✓ sig. —
Amyloidosis Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
1 gene
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ITM2B(1)
0.038 1.000 1.61e-3 2.26e-3 ✓ sig. —
Cerebral amyloid angiopathy Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(3)
0.014 1.000 4.58e-3 5.54e-3 ✓ sig. —
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Vascular dementia
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(2)
0.008 1.000 8.26e-3 9.40e-3 ✓ sig. —

Showing 5 of 5 matching pairs, sorted by significance (ascending). Click a column header to sort.