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
Hypertensive nephropathy Sebastian syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH9(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Dandy-walker syndrome SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETD2(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Dandy-walker syndrome SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETD2(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Congenital diaphragmatic hernia SIN3A-related intellectual disability syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SIN3A(3)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 343 →
Platelet-type bleeding disorder Sleep deprivation
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTGS1(3)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Parkinson-dementia syndrome Splenomegaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
MAPT(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 18 →
Platelet-type bleeding disorder platelet-type bleeding disorder 11
1 gene
Show details
1 of 1 corroborated by 2+ sources
GP6(6)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Platelet-type bleeding disorder platelet-type bleeding disorder 12
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTGS1(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Platelet-type bleeding disorder platelet-type bleeding disorder 15
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACTN1(6)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 33 →
Platelet-type bleeding disorder platelet-type bleeding disorder 17
1 gene
Show details
1 of 1 corroborated by 2+ sources
GFI1B(4)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Platelet-type bleeding disorder platelet-type bleeding disorder 18
1 gene
Show details
1 of 1 corroborated by 2+ sources
RASGRP2(7)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 33 →
Platelet-type bleeding disorder platelet-type bleeding disorder 20
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLFN14(6)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Platelet-type bleeding disorder platelet-type bleeding disorder 8
1 gene
Show details
1 of 1 corroborated by 2+ sources
P2RY12(6)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
primary ciliary dyskinesia 17 Situs inversus
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAAF19(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Fraser syndrome primary ciliary dyskinesia 20
1 gene
Show details
1 of 1 corroborated by 2+ sources
ODAD1(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 242 →
primary ciliary dyskinesia 3 Situs inversus
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAH5(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
primary ciliary dyskinesia 7 Situs inversus
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAH11(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Hypertensive nephropathy PRKAG2-related cardiomyopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
PRKAG2(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Intrahepatic cholestasis of pregnancy progressive familial intrahepatic cholestasis type 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCB4(4)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 319 →
Prolidase deficiency Splenomegaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
PEPD(3)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
focal segmental glomerulosclerosis 4, susceptibility to Hypertensive nephropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOL1(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
Fraser syndrome fraser syndrome 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
GRIP1(6)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —
FZD4-related exudative vitreoretinopathy Retinopathy of prematurity
1 gene
Show details
1 of 1 corroborated by 2+ sources
FZD4(3)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 288 →
Fraser syndrome Genetic infertility
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPATA22(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. Cluster 242 →
Cutis laxa glycogen storage disease due to glycogen branching enzyme deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GBE1(2)
0.048 1.000 1.30e-3 2.06e-3 ✓ sig. —

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