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
cardiomyopathy, dilated, 2e Ventricular fibrillation
1 gene
Show details
1 of 1 corroborated by 2+ sources
JPH2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 4 →
Congenital right-sided heart lesions Ventricular fibrillation
1 gene
Show details
SLC27A6(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 4 →
Coq7-related distal hereditary motor neuropathy Distal hereditary motor neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ7(5)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Coronary vessel anomalies Microphthalmos
1 gene
Show details
1 of 1 corroborated by 2+ sources
GCLC(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Corpus callosum agenesis with facial anomalies and robin sequence
1 gene
Show details
DDX3X(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
craniosynostosis 4 Ocular hypotension
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERF(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Complete unilateral cleft lip Deafness with labyrinthine aplasia, microtia, and microdontia
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF3(7)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Athabaskan brainstem dysgenesis syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
HOXA1(5)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
BBS9-related ciliopathy Smooth surface dental caries
1 gene
Show details
1 of 1 corroborated by 2+ sources
BBS9(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Focal dermal hypoplasia Microphthalmos
1 gene
Show details
1 of 1 corroborated by 2+ sources
PORCN(7)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 56 →
Brain infarction leukoencephalopathy with vanishing white matter 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF2B3(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay lissencephaly spectrum disorder with complex brainstem malformation
1 gene
Show details
1 of 1 corroborated by 2+ sources
MACF1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Complete unilateral cleft lip Merkel cell carcinoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYC(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
microphthalmia, syndromic 12 Microphthalmos
1 gene
Show details
1 of 1 corroborated by 2+ sources
RARB(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
17q11.2 microduplication syndrome Moyamoya angiopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
NF1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 77 →
Cervical lymphadenopathy Moyamoya angiopathy
1 gene
Show details
NF1(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 77 →
Moyamoya angiopathy Watson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NF1(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 77 →
HELIOS deficiency T-cell leukemia-lymphoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
IKZF2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 147 →
Distal hereditary motor neuropathy Hereditary axonal motor and sensory neuropathy
1 gene
Show details
BICD2(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Distal hereditary motor neuropathy hereditary peripheral neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
IGHMBP2(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Emphysema hermansky-pudlak syndrome 10
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP3D1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay hyperinsulinemic hypoglycemia with polycystic kidney disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
PMM2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
hypomagnesemia, seizures, and intellectual disability 1 Moyamoya angiopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CNNM2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Ichthyosis vulgaris
1 gene
Show details
1 of 1 corroborated by 2+ sources
FLG(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Naxos disease Ventricular fibrillation
1 gene
Show details
1 of 1 corroborated by 2+ sources
JUP(6)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —

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