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
Moyamoya angiopathy neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline
1 gene
Show details
1 of 1 corroborated by 2+ sources
CAPRIN1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Moyamoya angiopathy neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
CAPRIN1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Distal hereditary motor neuropathy neuronopathy, distal hereditary motor, autosomal dominant
1 gene
Show details
1 of 1 corroborated by 2+ sources
HSPB8(6)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Distal hereditary motor neuropathy neuronopathy, distal hereditary motor, autosomal recessive 5
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAJB2(7)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 15 →
Distal hereditary motor neuropathy neuronopathy, distal hereditary motor, type 7A
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC5A7(6)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Neurooculocardio-genitourinary syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
WDR37(6)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Complete unilateral cleft lip NOG-related symphalangism spectrum disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
NOG(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Emphysema Ocular albinism with sensorineural deafness
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP3D1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Choroidal neovascularization Ocular hypotension
1 gene
Show details
1 of 1 corroborated by 2+ sources
VEGFA(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Ocular hypotension Tongue disorder
1 gene
Show details
ESRRG(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Ocular hypotension Usher syndrome type 2D
1 gene
Show details
1 of 1 corroborated by 2+ sources
WHRN(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 84 →
Microphthalmos Orbital disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
RARB(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Complete unilateral cleft lip Osteolysis, hereditary, of carpal bones with or without nephropathy
1 gene
Show details
MAFB(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Complete unilateral cleft lip Otodental dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF3(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Developmental delay with or without epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPTAN1(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Diabetic macular edema Ocular hypotension
1 gene
Show details
MRPL19(1)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 84 →
Diets-jongmans syndrome syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
KDM3B(5)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 224 →
dilated cardiomyopathy 1BB Ventricular fibrillation
1 gene
Show details
1 of 1 corroborated by 2+ sources
DSG2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. Cluster 4 →
dilated cardiomyopathy 1HH Distal hereditary motor neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
BAG3(4)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
dilated cardiomyopathy 1W Ventricular fibrillation
1 gene
Show details
1 of 1 corroborated by 2+ sources
VCL(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Distal axonal motor neuropathy-myofibrillar myopathy syndrome Distal hereditary motor neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
HSPB8(6)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
OTUD6B(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Early-onset severe hermansky-pudlak syndrome with hearing loss due to ap3d1 deficiency Emphysema
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP3D1(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Moyamoya angiopathy Tetany
1 gene
Show details
1 of 1 corroborated by 2+ sources
CNNM2(2)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —
Learning disorders Thauvin-robinet-faivre syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FIBP(3)
0.027 1.000 2.34e-3 3.24e-3 ✓ sig. —

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