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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
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. —
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 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 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CD151(4)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CD151(5)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa occult macular dystrophy
1 gene
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1 of 1 corroborated by 2+ sources
RP1L1(2)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa Nephropathy with pretibial epidermolysis bullosa and deafness
1 gene
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1 of 1 corroborated by 2+ sources
CD151(5)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
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(8)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa Ulnar-fibular ray defect and brachydactyly
1 gene
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RP1L1(1)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa mucopolysaccharidosis type 2
1 gene
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1 of 1 corroborated by 2+ sources
IDS(2)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysis bullosa hereditary sensory and autonomic neuropathy type 6
1 gene
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1 of 1 corroborated by 2+ sources
DST(7)
0.045 1.000 1.36e-3 2.15e-3 ✓ sig. —
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
PLEC(8)
0.045 1.000 1.36e-3 2.15e-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 Sjogren-larsson syndrome
1 gene
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KRT14(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Bronchopulmonary dysplasia epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ITGA3(2)
0.022 1.000 2.92e-3 3.88e-3 ✓ sig. —
Bronchopulmonary dysplasia Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
1 gene
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ITGA3(1)
0.022 1.000 2.92e-3 3.88e-3 ✓ sig. —
Anemia epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ITGA3(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
1 gene
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ITGA3(1)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
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. —
Kindler epidermolysis bullosa Skin disease
1 gene
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1 of 1 corroborated by 2+ sources
FERMT1(2)
0.006 1.000 1.15e-2 1.29e-2 ✓ sig. —
Kindler epidermolysis bullosa Ulcerative colitis
1 gene
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1 of 1 corroborated by 2+ sources
FERMT1(2)
0.002 1.000 3.97e-2 4.15e-2 ✓ sig. —
Inflammatory bowel disease Kindler epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
FERMT1(2)
0.001 1.000 4.48e-2 4.66e-2 ✓ sig. —

Showing 25 of 76 matching pairs, sorted by significance (ascending). Click a column header to sort.