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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.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Dowling degos disease Weber-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KRT5(6)
0.111 0.250 1.30e-3 2.06e-3 ✓ sig. —
Cholestasis Cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC1(2)
0.111 0.333 1.17e-3 1.90e-3 ✓ sig. —
Cockayne syndrome Xfe progeroid syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC4(6)
0.125 0.500 7.79e-4 1.41e-3 ✓ sig. —
Xeroderma pigmentosum-cockayne syndrome Xfe progeroid syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC4(6)
0.143 0.500 6.49e-4 1.24e-3 ✓ sig. —
Sjogren-larsson syndrome Weber-cockayne syndrome
1 gene
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KRT14(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 269 →
Cockayne syndrome xeroderma pigmentosum group F
1 gene
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1 of 1 corroborated by 2+ sources
ERCC4(3)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
xeroderma pigmentosum group G Xeroderma pigmentosum-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC5(4)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. Cluster 86 →
xeroderma pigmentosum group F Xeroderma pigmentosum-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC4(3)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. —
xeroderma pigmentosum group D Xeroderma pigmentosum-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC2(3)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. Cluster 86 →
xeroderma pigmentosum group B Xeroderma pigmentosum-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ERCC3(4)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. Cluster 86 →
Dermatopathia pigmentosa reticularis Weber-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KRT14(6)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 269 →
Epidermolysis bullosa simplex Weber-cockayne syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KRT14(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 269 →
Salivary gland neoplasms Weber-cockayne syndrome
2 genes
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2 of 2 corroborated by 2+ sources
KRT5(2), ITGB4(2)
0.043 0.500 4.77e-5 2.16e-4 ✓ sig. —
Dysarthria Xeroderma pigmentosum-cockayne syndrome
2 genes
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1 of 2 corroborated by 2+ sources
BIVM-ERCC5(1), ERCC5(3)
0.077 0.400 1.94e-5 9.23e-5 ✓ sig. —
Cockayne syndrome Xeroderma pigmentosum
2 genes
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2 of 2 corroborated by 2+ sources
ERCC1(3), ERCC4(7)
0.118 0.333 8.34e-6 4.16e-5 ✓ sig. —
Trichothiodystrophy Xeroderma pigmentosum-cockayne syndrome
2 genes
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2 of 2 corroborated by 2+ sources
ERCC2(5), ERCC3(7)
0.133 0.400 4.63e-6 2.42e-5 ✓ sig. Cluster 86 →
Cockayne syndrome Testicular neoplasms
2 genes
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2 of 2 corroborated by 2+ sources
ERCC1(3), ERCC4(3)
0.167 0.333 2.65e-6 1.44e-5 ✓ sig. —
Galactokinase deficiency Weber-cockayne syndrome
2 genes
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1 of 2 corroborated by 2+ sources
ITGB4(1), GALK1(3)
0.286 0.500 3.04e-7 1.95e-6 ✓ sig. —
Cockayne syndrome De sanctis-cacchione syndrome
2 genes
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1 of 2 corroborated by 2+ sources
ERCC6(7), PGBD3(1)
0.286 1.000 1.27e-7 8.71e-7 ✓ sig. —
Epidermolysis bullosa Weber-cockayne syndrome
3 genes
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3 of 3 corroborated by 2+ sources
KRT5(7), ITGB4(5), KRT14(7)
0.130 0.750 8.74e-9 7.04e-8 ✓ sig. —
Cerebrooculofacioskeletal syndrome Cockayne syndrome
3 genes
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2 of 3 corroborated by 2+ sources
ERCC1(5), ERCC6(7), PGBD3(1)
0.300 0.500 6.57e-10 6.04e-9 ✓ sig. —
Cerebrooculofacioskeletal syndrome Xeroderma pigmentosum-cockayne syndrome
3 genes
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2 of 3 corroborated by 2+ sources
ERCC2(6), BIVM-ERCC5(1), ERCC5(6)
0.333 0.600 3.29e-10 3.12e-9 ✓ sig. Cluster 86 →
Junctional epidermolysis bullosa Weber-cockayne syndrome
4 genes
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1 of 4 corroborated by 2+ sources
KRT5(1), ITGB4(6), GALK1(1), KRT14(1)
0.211 1.000 1.31e-12 1.57e-11 ✓ sig. —
Cockayne syndrome Uv-sensitive syndrome
4 genes
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2 of 4 corroborated by 2+ sources
ERCC8(8), NDUFAF2(1), ERCC6(7), PGBD3(1)
0.500 0.800 3.20e-14 4.30e-13 ✓ sig. —
Xeroderma pigmentosum Xeroderma pigmentosum-cockayne syndrome
5 genes
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4 of 5 corroborated by 2+ sources
ERCC2(7), ERCC4(7), BIVM-ERCC5(1), ERCC5(7), ERCC3(7)
0.385 1.000 1.10e-16 1.76e-15 ✓ sig. Cluster 86 →

Showing 25 of 25 matching pairs, sorted by significance (descending). Click a column header to sort.