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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
Agenesis of corpus callosum Dejerine-sottas disease
1 gene
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1 of 1 corroborated by 2+ sources
SLC12A6(2)
0.025 0.500 4.93e-3 6.05e-3 ✓ sig. —
Agenesis of corpus callosum Auditory neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
CDH2(3)
0.030 0.500 4.02e-3 5.09e-3 ✓ sig. —
Agenesis of corpus callosum Cerebral arteriovenous malformations
1 gene
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1 of 1 corroborated by 2+ sources
CDH2(3)
0.042 0.500 2.86e-3 3.81e-3 ✓ sig. —
Agenesis of corpus callosum Clinodactyly
1 gene
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1 of 1 corroborated by 2+ sources
SLC12A6(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Congenital mirror movements Partial agenesis of corpus callosum
1 gene
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1 of 1 corroborated by 2+ sources
DCC(3)
0.143 0.333 7.79e-4 1.41e-3 ✓ sig. —
Mirror movements Partial agenesis of corpus callosum
1 gene
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1 of 1 corroborated by 2+ sources
DCC(6)
0.143 0.333 7.79e-4 1.41e-3 ✓ sig. —
Horizontal gaze palsy with progressive scoliosis Partial agenesis of corpus callosum
1 gene
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DCC(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Partial agenesis of corpus callosum Triphalangeal thumb-polysyndactyly syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SHH(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 232 →
Agenesis of corpus callosum Corpus callosum agenesis neuronopathy syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SLC12A6(4)
0.250 0.500 2.60e-4 6.51e-4 ✓ sig. —
holoprosencephaly 3 Partial agenesis of corpus callosum
1 gene
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1 of 1 corroborated by 2+ sources
SHH(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 232 →
Partial agenesis of corpus callosum Preaxial polydactyly with upper back hypertrichosis
1 gene
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1 of 1 corroborated by 2+ sources
SHH(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 232 →
Partial agenesis of corpus callosum Skeletal system disorder
1 gene
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SHH(1)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 232 →

Showing 12 of 12 matching pairs, sorted by significance (descending). Click a column header to sort.