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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
Bipolar disorder Congenital intrinsic factor deficiency
1 gene
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1 of 1 corroborated by 2+ sources
CBLIF(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder congenital disorder of glycosylation, type Iw, autosomal dominant
1 gene
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1 of 1 corroborated by 2+ sources
STT3A(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder combined immunodeficiency due to STK4 deficiency
1 gene
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1 of 1 corroborated by 2+ sources
STK4(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Blepharospasm
1 gene
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1 of 1 corroborated by 2+ sources
DRD5(3)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Braddock-carey syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KIF15(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Intellectual developmental disorder short stature facial speech
1 gene
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1 of 1 corroborated by 2+ sources
FBXL3(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Intellectual developmental disorder short stature facial
1 gene
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1 of 1 corroborated by 2+ sources
FBXL3(3)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Intellectual developmental disorder behavioral short stature
1 gene
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1 of 1 corroborated by 2+ sources
PUS7(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder inherited interstitial lung disease
1 gene
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1 of 1 corroborated by 2+ sources
LAMP3(2)
0.001 1.000 7.92e-2 8.03e-2 Cluster 2 →
Al kaissi syndrome Bipolar disorder
1 gene
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CDK10(1)
0.001 1.000 7.92e-2 8.03e-2 —
21q22.11q22.12 microdeletion syndrome Bipolar disorder
1 gene
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1 of 1 corroborated by 2+ sources
KIF15(3)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder STT3A-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
STT3A(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2
1 gene
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1 of 1 corroborated by 2+ sources
MOCS3(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder syndromic X-linked intellectual disability Siderius type
1 gene
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1 of 1 corroborated by 2+ sources
PHF8(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder retinitis pigmentosa 18
1 gene
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1 of 1 corroborated by 2+ sources
PRPF3(2)
0.001 1.000 7.92e-2 8.03e-2 Cluster 2 →
Bipolar disorder holocarboxylase synthetase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
HLCS(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder hypotaurinemic retinal degeneration and cardiomyopathy
1 gene
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1 of 1 corroborated by 2+ sources
SLC6A6(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Hypertryptophanemia
1 gene
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1 of 1 corroborated by 2+ sources
TDO2(6)
0.001 1.000 7.92e-2 8.03e-2 —
Progressive arterial occlusive disease with hypertension Ulcerative colitis
1 gene
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1 of 1 corroborated by 2+ sources
DAP3(2)
0.002 0.500 7.78e-2 7.90e-2 —
Obesity Pancreatic beta-cell agenesis with neonatal diabetes mellitus
1 gene
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1 of 1 corroborated by 2+ sources
PTF1A(2)
0.001 1.000 7.75e-2 7.87e-2 —
Obesity PLIN1-related familial partial lipodystrophy
1 gene
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1 of 1 corroborated by 2+ sources
PLIN1(3)
0.001 1.000 7.75e-2 7.87e-2 —
hawkinsinuria Obesity
1 gene
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1 of 1 corroborated by 2+ sources
HPD(2)
0.001 1.000 7.75e-2 7.87e-2 —
Hyperinflammatory lymphoproliferative immunodeficiency Obesity
1 gene
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1 of 1 corroborated by 2+ sources
NCKAP1L(2)
0.001 1.000 7.75e-2 7.87e-2 —
medium chain acyl-coa dehydrogenase deficiency Obesity
1 gene
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1 of 1 corroborated by 2+ sources
ACADM(3)
0.001 1.000 7.75e-2 7.87e-2 —
methylmalonate semialdehyde dehydrogenase deficiency Obesity
1 gene
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1 of 1 corroborated by 2+ sources
ALDH6A1(3)
0.001 1.000 7.75e-2 7.87e-2 —

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