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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
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. —
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 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. —
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. —
Dominant dystrophic epidermolysis bullosa, albopapular type Duane retraction syndrome
1 gene
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COL7A1(1)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 160 →
Dominant dystrophic epidermolysis bullosa with absence of skin Duane retraction syndrome
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 160 →
Epidermolysis bullosa simplex Tongue neoplasms
1 gene
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1 of 1 corroborated by 2+ sources
KRT14(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 269 →
Anonychia Dystrophic epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(8)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 160 →
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Other epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
PLEC(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Other 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(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Epidermolysis bullosa Fraser syndrome
2 genes
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1 of 2 corroborated by 2+ sources
FREM2(6), BCLAF1(1)
0.050 0.100 3.32e-4 7.87e-4 ✓ sig. —
Aplasia cutis congenita PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder
1 gene
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1 of 1 corroborated by 2+ sources
PLEC(3)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. —
Dystrophic epidermolysis bullosa Hallopeau siemens disease
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(8)
0.250 0.500 2.60e-4 6.51e-4 ✓ sig. Cluster 160 →
Dystrophic epidermolysis bullosa Nail dystrophy
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(8)
0.250 0.500 2.60e-4 6.51e-4 ✓ sig. Cluster 160 →
Lethal acantholytic epidermolysis bullosa Ventricular arrhythmia
1 gene
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1 of 1 corroborated by 2+ sources
DSP(3)
0.250 0.500 2.60e-4 6.51e-4 ✓ sig. Cluster 201 →
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 →
Anonychia Dominant dystrophic epidermolysis bullosa, albopapular type
1 gene
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COL7A1(1)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 160 →
Anonychia Dominant dystrophic epidermolysis bullosa with absence of skin
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 160 →
Lethal acantholytic epidermolysis bullosa Naxos disease
1 gene
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1 of 1 corroborated by 2+ sources
JUP(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 201 →
Carvajal syndrome Lethal acantholytic epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
DSP(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 201 →
arrhythmogenic cardiomyopathy with wooly hair and keratoderma Lethal acantholytic epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
DSP(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 201 →
Erythrokeratodermia-cardiomyopathy syndrome Lethal acantholytic epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
DSP(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 201 →
Dominant dystrophic epidermolysis bullosa with absence of skin Dystrophic epidermolysis bullosa
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(8)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 160 →

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