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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
Complex partial epilepsy genetic developmental and epileptic encephalopathy
1 gene
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1 of 1 corroborated by 2+ sources
SCN3A(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Congenital brain dysgenesis due to glutamine synthetase deficiency genetic developmental and epileptic encephalopathy
1 gene
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1 of 1 corroborated by 2+ sources
GLUL(5)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
genetic developmental and epileptic encephalopathy self-limited familial neonatal epilepsy
1 gene
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KCNQ3(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Epilepsy of infancy with migrating focal seizures genetic developmental and epileptic encephalopathy
4 genes
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4 of 4 corroborated by 2+ sources
SCN1A(2), SLC12A5(3), PLCB1(2), SLC25A22(2)
0.095 0.444 3.14e-9 2.70e-8 ✓ sig. —
genetic developmental and epileptic encephalopathy Malignant migrating partial seizures of infancy
4 genes
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4 of 4 corroborated by 2+ sources
SCN1A(3), SLC12A5(3), PLCB1(3), SLC25A22(3)
0.095 0.444 3.14e-9 2.70e-8 ✓ sig. —
genetic developmental and epileptic encephalopathy Rolandic epilepsy
8 genes
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8 of 8 corroborated by 2+ sources
WWOX(2), SZT2(2), SCN1A(2), SCN1B(2), KCNQ3(2), CSTB(2), PLCB1(2), SPTAN1(2)
0.105 0.222 1.14e-13 1.47e-12 ✓ sig. —
genetic developmental and epileptic encephalopathy West syndrome
8 genes
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8 of 8 corroborated by 2+ sources
WWOX(2), SIK1(2), ARX(2), SCN1A(2), DNM1(2), STXBP1(2), PLCB1(2), SPTAN1(2)
0.136 0.267 2.18e-15 3.19e-14 ✓ sig. —
Developmental and epileptic encephalopathy genetic developmental and epileptic encephalopathy
36 genes
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36 of 36 corroborated by 2+ sources
WWOX(6), ABAT(3), CACNA1E(6), CUX2(6), PACS2(6), SIK1(6), SYNJ1(6), SZT2(7), GLUL(6), RYR3(3), ITPA(6), GABRB3(6) +24 more
0.163 1.000 1.90e-68 1.34e-66 ✓ sig. —

Showing 8 of 8 matching pairs, sorted by significance (descending). Click a column header to sort.