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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
Dowling degos disease Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
KRT5(6)
0.043 0.200 5.83e-3 7.05e-3 ✓ sig. —
Junctional epidermolysis bullosa Sjogren-larsson syndrome
1 gene
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KRT14(1)
0.050 0.500 2.34e-3 3.24e-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. —
Junctional epidermolysis bullosa Salivary gland neoplasms
2 genes
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2 of 2 corroborated by 2+ sources
KRT5(2), ITGB4(6)
0.033 0.111 1.19e-3 1.92e-3 ✓ sig. —
epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
ITGA3(7)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Junctional epidermolysis bullosa PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder
1 gene
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1 of 1 corroborated by 2+ sources
PLEC(4)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Junctional epidermolysis bullosa Naxos disease
1 gene
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1 of 1 corroborated by 2+ sources
JUP(6)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Junctional epidermolysis bullosa Laryngo-onycho-cutaneous syndrome
1 gene
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1 of 1 corroborated by 2+ sources
LAMA3(7)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Hearing loss with hypertrophic cardiomyopathy Junctional epidermolysis bullosa
1 gene
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MYO6(1)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Epidermolysis bullosa simplex Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
KRT14(2)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
PLEC(4)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Dermatopathia pigmentosa reticularis Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
KRT14(6)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Congenital phimosis Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
ITGA3(7)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome Junctional epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
ITGA3(7)
0.053 1.000 1.17e-3 1.90e-3 ✓ sig. —
Junctional epidermolysis bullosa Lethal acantholytic epidermolysis bullosa
2 genes
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2 of 2 corroborated by 2+ sources
JUP(3), DSP(5)
0.105 1.000 1.29e-6 7.42e-6 ✓ sig. —
Amelogenesis imperfecta Junctional epidermolysis bullosa
4 genes
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4 of 4 corroborated by 2+ sources
COL7A1(4), COL17A1(7), LAMB3(6), LAMC2(6)
0.100 0.222 1.63e-8 1.28e-7 ✓ sig. —
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. —
Junctional epidermolysis bullosa Other epidermolysis bullosa
6 genes
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6 of 6 corroborated by 2+ sources
PLEC(3), COL17A1(7), LAMB3(6), LAMC2(6), ITGB4(6), ITGA6(6)
0.316 1.000 1.00e-18 1.78e-17 ✓ sig. —
Epidermolysis bullosa Junctional epidermolysis bullosa
8 genes
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8 of 8 corroborated by 2+ sources
COL7A1(6), PLEC(8), LAMB3(6), KRT5(7), ITGB4(7), ITGA6(7), KRT14(7), KLHL24(6)
0.250 0.444 1.13e-19 2.12e-18 ✓ sig. —

Showing 19 of 19 matching pairs, sorted by significance (descending). Click a column header to sort.