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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
Acral peeling skin syndrome Lung cancer
1 gene
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1 of 1 corroborated by 2+ sources
TGM5(2)
0.002 0.500 8.25e-2 8.37e-2 —
Acral peeling skin syndrome Glioblastoma
1 gene
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1 of 1 corroborated by 2+ sources
CSTA(2)
0.002 0.500 7.73e-2 7.86e-2 —
Hypotrichosis Peeling skin syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CDSN(7)
0.042 0.143 7.70e-3 9.00e-3 ✓ sig. —
Cutaneous lupus erythematosus Peeling skin syndrome
1 gene
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1 of 1 corroborated by 2+ sources
0.056 0.143 4.99e-3 6.12e-3 ✓ sig. —
Peeling skin syndrome with leukonychia and acral punctate keratoses Vasculitis
1 gene
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1 of 1 corroborated by 2+ sources
CAST(6)
0.032 0.500 3.76e-3 4.81e-3 ✓ sig. —
Aneurysm Peeling skin syndrome with leukonychia and acral punctate keratoses
1 gene
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1 of 1 corroborated by 2+ sources
CAST(7)
0.034 0.500 3.50e-3 4.52e-3 ✓ sig. —
Blood coagulation disorder Peeling skin syndrome with leukonychia and acral punctate keratoses
1 gene
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1 of 1 corroborated by 2+ sources
CAST(7)
0.038 0.500 3.11e-3 4.10e-3 ✓ sig. —
Acral peeling skin syndrome Nasopharyngeal carcinoma
1 gene
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1 of 1 corroborated by 2+ sources
CSTA(2)
0.042 0.500 2.86e-3 3.81e-3 ✓ sig. —
Acral peeling skin syndrome Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
CSTA(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Peeling skin syndrome with leukonychia and acral punctate keratoses Pemphigus
1 gene
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1 of 1 corroborated by 2+ sources
CAST(6)
0.100 0.500 1.04e-3 1.74e-3 ✓ sig. Cluster 1 →
Peeling skin syndrome Rheumatic disease
2 genes
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2 of 2 corroborated by 2+ sources
PSORS1C1(2), CDSN(7)
0.105 0.286 1.38e-5 6.66e-5 ✓ sig. —
Hypotrichosis simplex Peeling skin syndrome
2 genes
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1 of 2 corroborated by 2+ sources
PSORS1C1(1), CDSN(7)
0.111 0.286 1.17e-5 5.71e-5 ✓ sig. —
Peeling skin syndrome with leukonychia and acral punctate keratoses Uveitis
2 genes
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2 of 2 corroborated by 2+ sources
CAST(7), ERAP1(2)
0.059 1.000 4.45e-6 2.34e-5 ✓ sig. —
Acral peeling skin syndrome Peeling skin syndrome
2 genes
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2 of 2 corroborated by 2+ sources
CSTA(4), TGM5(4)
0.250 1.000 1.77e-7 1.18e-6 ✓ sig. —

Showing 14 of 14 matching pairs, sorted by significance (descending). Click a column header to sort.