Log in to save this analysis

Save This Analysis

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 Cerebral arterial disease
1 gene
Show details
ADGRE3(1)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Cerebrofacial arteriovenous metameric syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNA14(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Charcot-Marie-Tooth disease, axonal, type 2FF
1 gene
Show details
1 of 1 corroborated by 2+ sources
CADM3(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder X-linked epilepsy with or without intellectual disability and dysmorphic features
1 gene
Show details
1 of 1 corroborated by 2+ sources
GABRA3(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder leukodystrophy, hypomyelinating, 22
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLDN11(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Maleylacetoacetate isomerase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GSTZ1(5)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder inherited interstitial lung disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
LAMP3(2)
0.001 1.000 7.92e-2 8.03e-2 Cluster 2 →
Bipolar disorder Intellectual developmental disorder behavioral short stature
1 gene
Show details
1 of 1 corroborated by 2+ sources
PUS7(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Intellectual developmental disorder short stature facial
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBXL3(3)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Intellectual developmental disorder short stature facial speech
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBXL3(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder retinitis pigmentosa 18
1 gene
Show details
1 of 1 corroborated by 2+ sources
PRPF3(2)
0.001 1.000 7.92e-2 8.03e-2 Cluster 2 →
Bipolar disorder STT3A-congenital disorder of glycosylation
1 gene
Show details
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
Show details
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
Show details
1 of 1 corroborated by 2+ sources
PHF8(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder dyskeratosis congenita and related telomere biology disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
RPA1(2)
0.001 1.000 7.92e-2 8.03e-2 —
autosomal dominant cerebellar ataxia Bipolar disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
NPTX1(2)
0.001 1.000 7.92e-2 8.03e-2 —
Benign essential blepharospasm Bipolar disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
DRD5(2)
0.001 1.000 7.92e-2 8.03e-2 —
21q22.11q22.12 microdeletion syndrome Bipolar disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIF15(3)
0.001 1.000 7.92e-2 8.03e-2 —
Al kaissi syndrome Bipolar disorder
1 gene
Show details
CDK10(1)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Oculocerebrodental syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIK3C2A(3)
0.001 1.000 7.92e-2 8.03e-2 Cluster 2 →
Bipolar disorder Blepharospasm
1 gene
Show details
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
Show details
1 of 1 corroborated by 2+ sources
KIF15(4)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder holocarboxylase synthetase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
HLCS(2)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder Hypertryptophanemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TDO2(6)
0.001 1.000 7.92e-2 8.03e-2 —
Bipolar disorder hypotaurinemic retinal degeneration and cardiomyopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC6A6(2)
0.001 1.000 7.92e-2 8.03e-2 —

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