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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
inherited blood coagulation disorder Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
APOLD1(2)
0.001 1.000 6.24e-2 6.39e-2 —
kidney disorder Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
SLC41A1(2)
0.001 1.000 6.24e-2 6.39e-2 —
DPM3-congenital disorder of glycosylation Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
DPM3(2)
0.001 1.000 6.24e-2 6.39e-2 —
dyskeratosis congenita and related telomere biology disorder Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
RPA1(2)
0.001 1.000 6.24e-2 6.39e-2 —
Prostate cancer Thrombocytopenia with platelet secretion defect
1 gene
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1 of 1 corroborated by 2+ sources
SLFN14(3)
0.001 1.000 6.24e-2 6.39e-2 —
Prostate cancer thrombotic disease
1 gene
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1 of 1 corroborated by 2+ sources
MAST2(2)
0.001 1.000 6.24e-2 6.39e-2 —
Prostate cancer tooth agenesis, selective, 3
1 gene
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1 of 1 corroborated by 2+ sources
PAX9(3)
0.001 1.000 6.24e-2 6.39e-2 —
bleeding disorder, platelet-type, 22 Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
EPHB2(4)
0.001 1.000 6.24e-2 6.39e-2 —
combined immunodeficiency due to GINS1 deficiency Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
GINS1(2)
0.001 1.000 6.24e-2 6.39e-2 —
congenital disorder of glycosylation type 1E Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
DPM1(2)
0.001 1.000 6.24e-2 6.39e-2 —
leukodystrophy, hypomyelinating, 18 Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
DEGS1(2)
0.001 1.000 6.24e-2 6.39e-2 —
leukodystrophy, hypomyelinating, 22 Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
CLDN11(2)
0.001 1.000 6.24e-2 6.39e-2 —
platelet-type bleeding disorder 20 Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
SLFN14(2)
0.001 1.000 6.24e-2 6.39e-2 —
Prostate cancer RAD51D-related cancer predisposition
1 gene
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1 of 1 corroborated by 2+ sources
RAD51D(2)
0.001 1.000 6.24e-2 6.39e-2 —
hyper-IgE recurrent infection syndrome 3, autosomal recessive Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
ZNF341(2)
0.001 1.000 6.24e-2 6.39e-2 —
3-hydroxyisobutyric aciduria Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
HIBADH(3)
0.001 1.000 6.24e-2 6.39e-2 —
Osteocraniostenosis Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
FAM111A(4)
0.001 1.000 6.24e-2 6.39e-2 —
FAM111A-related skeletal dysplasia Prostate cancer
1 gene
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1 of 1 corroborated by 2+ sources
FAM111A(2)
0.001 1.000 6.24e-2 6.39e-2 —
Color vision deficiency GNAT2-related retinopathy
1 gene
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1 of 1 corroborated by 2+ sources
GNAT2(3)
0.001 1.000 6.27e-2 6.42e-2 —
Color vision deficiency goldberg-shprintzen syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KIFBP(2)
0.001 1.000 6.27e-2 6.42e-2 —
colobomatous microphthalmia-rhizomelic dysplasia syndrome Color vision deficiency
1 gene
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1 of 1 corroborated by 2+ sources
MAB21L2(2)
0.001 1.000 6.27e-2 6.42e-2 —
Color vision deficiency dilated cardiomyopathy 2B
1 gene
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1 of 1 corroborated by 2+ sources
GATAD1(2)
0.001 1.000 6.27e-2 6.42e-2 —
Color vision deficiency immunodeficiency 76
1 gene
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1 of 1 corroborated by 2+ sources
FCHO1(2)
0.001 1.000 6.27e-2 6.42e-2 —
Color vision deficiency Inflammatory demyelinating polyneuropathy
1 gene
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CNBD1(1)
0.001 1.000 6.27e-2 6.42e-2 —
Biliary-renal-neuro-skeletal syndrome Color vision deficiency
1 gene
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1 of 1 corroborated by 2+ sources
IFT56(4)
0.001 1.000 6.27e-2 6.42e-2 —

Showing 25 of 20813 pairs, sorted by significance (ascending). Click a column header to sort.