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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
Centronuclear myopathy Congenital structural myopathy
8 genes
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6 of 8 corroborated by 2+ sources
BIN1(4), MTM1(1), MTMR14(3), RYR1(3), TPM3(1), DNM2(4), MYF6(2), CCDC78(3)
0.296 0.667 2.02e-21 4.06e-20 ✓ sig. Cluster 189 →
Congenital fiber type disproportion myopathy Congenital structural myopathy
3 genes
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1 of 3 corroborated by 2+ sources
MTM1(1), RYR1(1), TPM3(3)
0.143 0.273 5.95e-8 4.33e-7 ✓ sig. Cluster 189 →
Congenital structural myopathy Nemaline myopathy
3 genes
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2 of 3 corroborated by 2+ sources
ANKRD1(1), NEB(7), TPM3(4)
0.107 0.250 2.93e-7 1.90e-6 ✓ sig. —
Congenital structural myopathy X-linked centronuclear myopathy
2 genes
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1 of 2 corroborated by 2+ sources
MTM1(2), DNM2(1)
0.154 1.000 5.57e-7 3.41e-6 ✓ sig. —
Congenital structural myopathy Tubular aggregate myopathy
2 genes
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2 of 2 corroborated by 2+ sources
ORAI1(4), STIM1(4)
0.111 0.286 1.17e-5 5.71e-5 ✓ sig. —
combined immunodeficiency due to STIM1 deficiency Congenital structural myopathy
1 gene
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1 of 1 corroborated by 2+ sources
STIM1(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Congenital generalized hypercontractile muscle stiffness syndrome Congenital structural myopathy
1 gene
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1 of 1 corroborated by 2+ sources
TPM3(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Congenital structural myopathy TPM3-related myopathy
1 gene
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1 of 1 corroborated by 2+ sources
TPM3(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Congenital structural myopathy X-linked myotubular myopathy
1 gene
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1 of 1 corroborated by 2+ sources
MTM1(4)
0.071 0.500 1.56e-3 2.38e-3 ✓ sig. —

Showing 9 of 9 matching pairs, sorted by significance (ascending). Click a column header to sort.