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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
Concentric hypertrophic cardiomyopathy Short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CACNA1C(3)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Andersen-tawil syndrome Short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KCNJ2(6)
0.077 0.500 1.43e-3 2.23e-3 ✓ sig. —
Short qt syndrome Timothy syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CACNA1C(7)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Short qt syndrome Systemic primary carnitine deficiency
1 gene
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1 of 1 corroborated by 2+ sources
SLC22A5(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Repolarization syndrome Short qt syndrome
1 gene
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CACNB2(1)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
dilated cardiomyopathy 1W Short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
VCL(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Carnitine deficiency Short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SLC22A5(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Cardiogenetic disease Short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CACNB2(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital short qt syndrome Haploinsufficiency
1 gene
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1 of 1 corroborated by 2+ sources
KCNH2(2)
0.143 0.500 6.49e-4 1.24e-3 ✓ sig. —
Congenital short qt syndrome Jervell and lange-nielsen syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KCNQ1(7)
0.143 0.500 6.49e-4 1.24e-3 ✓ sig. —
Andersen-tawil syndrome Congenital short qt syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KCNJ2(5)
0.143 0.500 6.49e-4 1.24e-3 ✓ sig. —
Paroxysmal atrial fibrillation Short qt syndrome
2 genes
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2 of 2 corroborated by 2+ sources
KCNQ1(6), CACNA2D1(2)
0.143 0.500 2.78e-6 1.51e-5 ✓ sig. —
Congenital short qt syndrome Long qt syndrome, digenic
2 genes
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2 of 2 corroborated by 2+ sources
KCNH2(2), KCNQ1(2)
0.222 0.400 8.43e-7 5.00e-6 ✓ sig. —
Congenital short qt syndrome Paroxysmal atrial fibrillation
2 genes
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2 of 2 corroborated by 2+ sources
KCNQ1(2), CACNA2D1(2)
0.250 0.500 5.06e-7 3.14e-6 ✓ sig. —
Cardiac conduction disease Short qt syndrome
3 genes
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CACNB2(1), TRPM4(1), SCN5A(1)
0.167 0.333 2.27e-8 1.77e-7 ✓ sig. —
Long qt syndrome, digenic Short qt syndrome
3 genes
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2 of 3 corroborated by 2+ sources
KCNH2(5), KCNQ1(6), SCN5A(1)
0.214 0.600 2.71e-9 2.34e-8 ✓ sig. —
Conduction disorder of the heart Short qt syndrome
5 genes
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3 of 5 corroborated by 2+ sources
TRPM4(1), CACNA1C(3), KCNH2(5), KCNQ1(6), SCN5A(1)
0.161 0.455 2.71e-12 3.11e-11 ✓ sig. —
Congenital short qt syndrome Short qt syndrome
5 genes
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5 of 5 corroborated by 2+ sources
KCNJ2(6), KCNH2(6), KCNQ1(7), CACNA2D1(3), SLC4A3(6)
0.417 1.000 6.41e-17 1.04e-15 ✓ sig. —
Short qt syndrome Ventricular fibrillation
8 genes
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5 of 8 corroborated by 2+ sources
CACNB2(1), TRPM4(1), KCNJ2(6), CACNA1C(3), KCNH2(5), SCN5A(3), CACNA2D1(2), VCL(1)
0.200 0.727 6.35e-20 1.21e-18 ✓ sig. —

Showing 19 of 19 matching pairs, sorted by significance (descending). Click a column header to sort.