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
Chorea Continuous spike and wave during slow wave sleep syndrome
1 gene
Show details
FRRS1L(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Corpus callosum agenesis Seckel syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Clinodactyly Corpus callosum agenesis neuronopathy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC12A6(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Corneal neovascularization Thyroid hormone resistance
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRHR(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Seckel syndrome Urethral syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
syndromic complex neurodevelopmental disorder Ververi-brady syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
QRICH1(5)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. Cluster 109 →
Clinodactyly Wilson-turner syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HDAC8(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Hematologic disease Rhabdoid tumor
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMARCB1(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Junctional epidermolysis bullosa Sjogren-larsson syndrome
1 gene
Show details
KRT14(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Birk-barel syndrome syndromic complex neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPM3(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. Cluster 109 →
Cataract-glaucoma syndrome syndromic complex neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPM3(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. Cluster 109 →
Gross motor development delay Hemorrhagic stroke
1 gene
Show details
1 of 1 corroborated by 2+ sources
PDGFA(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Fetal erythroblastosis Giant cell arteritis
1 gene
Show details
FCGR2A(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Gm1 gangliosidosis Spondyloepiphyseal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLB1(6)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Intellectual developmental disorder dysmorphic cerebellar Melas syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYTB(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Intellectual developmental disorder dysmorphic ptosis syndromic complex neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
BRPF1(6)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. Cluster 109 →
Corneal neovascularization Intestinal polyposis
1 gene
Show details
1 of 1 corroborated by 2+ sources
STK11(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Dyssegmental dysplasia Spondyloepiphyseal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HSPG2(4)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Lipodystrophy non-severe combined immunodeficiency due to polymerase delta deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLD1(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Corneal neovascularization Ovarian hyperstimulation syndrome
1 gene
Show details
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Bifid uvula Clinodactyly
1 gene
Show details
ARF3(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
17p13.3 microduplication syndrome Carcinogenesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Acral peeling skin syndrome Junctional epidermolysis bullosa
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSTA(3)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Agenesis of corpus callosum Clinodactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC12A6(2)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —
Aortic atherosclerosis Diabetic nephropathy type 2
1 gene
Show details
NYAP2(1)
0.050 0.500 2.34e-3 3.24e-3 ✓ sig. —

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