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
Neurodevelopmental disorder Ververi-brady syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SEPHS1(3)
0.001 0.500 1.18e-1 1.19e-1 —
Central nervous system malformation Neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
LMNB2(2)
0.001 0.500 1.18e-1 1.19e-1 —
Nephronophthisis-like nephropathy Prostate cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC41A1(4)
0.001 0.500 1.21e-1 1.22e-1 —
Color vision deficiency White spongue nevus
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRT13(5)
0.001 0.500 1.22e-1 1.23e-1 —
Major depressive disorder TRIP11-related skeletal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIP11(2)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Vibratory urticaria
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADGRE2(6)
0.001 1.000 1.27e-1 1.28e-1 Cluster 2 →
Major depressive disorder Wernicke encephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TKT(3)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Yoon-bellen neurodevelopmental syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
OGDHL(3)
0.001 1.000 1.27e-1 1.28e-1 —
Major depressive disorder Zinc deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC30A2(4)
0.001 1.000 1.27e-1 1.28e-1 Cluster 2 →
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 —
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 —
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 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 —
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 —
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 —
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 —
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 —
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 —
Cayman type cerebellar ataxia Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATCAY(2)
0.001 1.000 1.27e-1 1.28e-1 —
chondrodysplasia with joint dislocations, gpapp type Major depressive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
BPNT2(2)
0.001 1.000 1.27e-1 1.28e-1 —

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