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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
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic
1 gene
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RHOA(1)
0.500 1.000 6.46e-5 1.98e-4 ✓ sig. —
Congenital hemihypertrophy Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
1 gene
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1 of 1 corroborated by 2+ sources
RHOA(2)
0.250 1.000 1.94e-4 4.41e-4 ✓ sig. —
Congenital hemihypertrophy Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic
1 gene
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1 of 1 corroborated by 2+ sources
RHOA(2)
0.250 1.000 1.94e-4 4.41e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies Peritoneal well differentiated papillary mesothelioma
1 gene
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RHOA(1)
0.250 1.000 1.94e-4 4.41e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic Peritoneal well differentiated papillary mesothelioma
1 gene
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RHOA(1)
0.250 1.000 1.94e-4 4.41e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies Peritoneal solitary fibrous tumor
1 gene
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RHOA(1)
0.167 1.000 3.23e-4 6.41e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic Peritoneal solitary fibrous tumor
1 gene
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RHOA(1)
0.167 1.000 3.23e-4 6.41e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies Placental site trophoblastic tumor
1 gene
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RHOA(1)
0.143 1.000 3.87e-4 7.33e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic Placental site trophoblastic tumor
1 gene
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RHOA(1)
0.143 1.000 3.87e-4 7.33e-4 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies Tooth disease
1 gene
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1 of 1 corroborated by 2+ sources
RHOA(3)
0.053 1.000 1.16e-3 1.73e-3 ✓ sig. —
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic Tooth disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
RHOA(3)
0.053 1.000 1.16e-3 1.73e-3 ✓ sig. —

Showing 11 of 11 matching pairs, sorted by significance (ascending). Click a column header to sort.