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
Coronary artery disease Ververi-brady syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
QRICH1(5)
0.001 0.500 1.43e-1 1.44e-1 —
Coronary artery disease Ear disorder
1 gene
Show details
SCML4(1)
0.001 0.500 1.43e-1 1.44e-1 —
Anauxetic dysplasia Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
POP1(5)
0.002 0.250 1.39e-1 1.41e-1 —
Attention deficit hyperactivity disorder Fructokinase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CGREF1(2)
0.001 0.500 1.38e-1 1.40e-1 —
2,4-dienoyl-coa reductase deficiency Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
DECR1(3)
0.001 0.500 1.35e-1 1.36e-1 —
Carnitine acetyltransferase deficiency Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.001 0.500 1.35e-1 1.36e-1 —
Breast cancer Keratosis palmoplantaris papulosa
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL14A1(2)
0.001 0.500 1.34e-1 1.35e-1 —
adult neuronal ceroid lipofuscinosis Breast cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTSF(2)
0.001 0.500 1.34e-1 1.35e-1 —
Ear disorder Scoliosis
1 gene
Show details
SCML4(1)
0.001 0.500 1.30e-1 1.31e-1 Cluster 2 →
BBS4-related ciliopathy Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
BBS4(2)
0.001 1.000 1.27e-1 1.28e-1 —
band heterotopia of brain Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
EML1(2)
0.001 1.000 1.27e-1 1.28e-1 —
Congenital isolated acth deficiency Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBX19(4)
0.001 1.000 1.27e-1 1.28e-1 —
Galactose mutarotase deficiency Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
GALM(2)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder primary ciliary dyskinesia 9
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAI2(2)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Peho-like syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CCDC88A(5)
0.001 1.000 1.27e-1 1.28e-1 —
hypotaurinemic retinal degeneration and cardiomyopathy Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC6A6(2)
0.001 1.000 1.27e-1 1.28e-1 —
hyperphenylalaninemia due to DNAJC12 deficiency Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAJC12(2)
0.001 1.000 1.27e-1 1.28e-1 —
hereditary leiomyomatosis and renal cell cancer Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
FH(2)
0.001 1.000 1.27e-1 1.28e-1 —
Copper metabolism disorder Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
CCS(2)
0.001 1.000 1.27e-1 1.28e-1 —
Corticosteroid-binding globulin deficiency Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Mak-related retinopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
MAK(3)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder SNRNP200-related dominant retinopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Telangiectasia–intellectual disability–microcephaly–metaphyseal dysplasia–eye abnormalities–short stature syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
LRRC8C(3)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive 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 1.27e-1 1.28e-1 —
Major depressive disorder systemic lupus erythematosus 17
1 gene
Show details
1 of 1 corroborated by 2+ sources
TLR7(2)
0.001 1.000 1.27e-1 1.28e-1 —

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