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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
Gout meier-gorlin syndrome 2
1 gene
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1 of 1 corroborated by 2+ sources
ORC4(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout Intellectual developmental disorder peripheral neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
NUDT2(5)
0.001 1.000 5.32e-2 5.48e-2 —
Gout neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
1 gene
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1 of 1 corroborated by 2+ sources
MED27(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout obsolete glaucoma 1, open angle, F
1 gene
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1 of 1 corroborated by 2+ sources
ASB10(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout Osteomalacia
1 gene
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1 of 1 corroborated by 2+ sources
MEPE(3)
0.001 1.000 5.32e-2 5.48e-2 —
Gout RFT1-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
RFT1(2)
0.001 1.000 5.32e-2 5.48e-2 —
Alpha-2-plasmin inhibitor deficiency Gout
1 gene
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1 of 1 corroborated by 2+ sources
0.001 1.000 5.32e-2 5.48e-2 —
Gout thrombocytopenia-absent radius syndrome
1 gene
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1 of 1 corroborated by 2+ sources
RBM8A(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout Wernicke encephalopathy
1 gene
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1 of 1 corroborated by 2+ sources
TKT(3)
0.001 1.000 5.32e-2 5.48e-2 —
glycogen storage disease I Gout
1 gene
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1 of 1 corroborated by 2+ sources
G6PC1(2)
0.001 1.000 5.32e-2 5.48e-2 —
glycogen storage disease V Gout
1 gene
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1 of 1 corroborated by 2+ sources
PYGM(2)
0.001 1.000 5.32e-2 5.48e-2 —
GNAT2-related retinopathy Gout
1 gene
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1 of 1 corroborated by 2+ sources
GNAT2(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout GPR161-related medulloblastoma predisposition
1 gene
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1 of 1 corroborated by 2+ sources
GPR161(2)
0.001 1.000 5.32e-2 5.48e-2 —
Gout Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
HPRT1(3)
0.001 1.000 5.32e-2 5.48e-2 —
Gout pyruvate kinase deficiency of red cells
1 gene
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1 of 1 corroborated by 2+ sources
PKLR(2)
0.001 1.000 5.32e-2 5.48e-2 —
Combined low ldl and fibrinogen Gout
1 gene
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1 of 1 corroborated by 2+ sources
B4GALT1(3)
0.001 1.000 5.32e-2 5.48e-2 —
Congenital alpha-2-antiplasmin deficiency Gout
1 gene
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1 of 1 corroborated by 2+ sources
0.001 1.000 5.32e-2 5.48e-2 —
congenital disorder of glycosylation with defective fucosylation 1 Gout
1 gene
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1 of 1 corroborated by 2+ sources
FUT8(2)
0.001 1.000 5.32e-2 5.48e-2 —
Congenital glucose-galactose malabsorption Gout
1 gene
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1 of 1 corroborated by 2+ sources
SLC5A1(3)
0.001 1.000 5.32e-2 5.48e-2 —
B4GALT1-congenital disorder of glycosylation Gout
1 gene
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1 of 1 corroborated by 2+ sources
B4GALT1(2)
0.001 1.000 5.32e-2 5.48e-2 —
Congenital plasmin inhibitor deficiency Gout
1 gene
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1 of 1 corroborated by 2+ sources
0.001 1.000 5.32e-2 5.48e-2 —
Dalmatian hypouricemia Gout
1 gene
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1 of 1 corroborated by 2+ sources
0.001 1.000 5.32e-2 5.48e-2 —
Diffuse cerebral and cerebellar atrophy–intractable seizures–progressive microcephaly syndrome Gout
1 gene
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1 of 1 corroborated by 2+ sources
QARS1(5)
0.001 1.000 5.32e-2 5.48e-2 —
DPM3-congenital disorder of glycosylation Gout
1 gene
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1 of 1 corroborated by 2+ sources
DPM3(2)
0.001 1.000 5.32e-2 5.48e-2 —
ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type Gout
1 gene
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1 of 1 corroborated by 2+ sources
KDF1(2)
0.001 1.000 5.32e-2 5.48e-2 —

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