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
Maleylacetoacetate isomerase deficiency Vestibular disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
GSTZ1(5)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
MCM9-related gametogenic failure Ovarian dysgenesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MCM9(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 38 →
familial thoracic aortic aneurysm and aortic dissection meester-loeys syndrome
1 gene
Show details
BGN(1)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Ear, patella, short stature syndrome meier-gorlin syndrome 2
1 gene
Show details
1 of 1 corroborated by 2+ sources
ORC4(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 171 →
Ear, patella, short stature syndrome meier-gorlin syndrome 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
ORC6(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 171 →
Ear, patella, short stature syndrome meier-gorlin syndrome 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDT1(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 171 →
Ear, patella, short stature syndrome meier-gorlin syndrome 6
1 gene
Show details
1 of 1 corroborated by 2+ sources
GMNN(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 171 →
MERTK-related retinopathy Thromboembolism
1 gene
Show details
1 of 1 corroborated by 2+ sources
MERTK(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 55 →
methylmalonic acidemia due to transcobalamin receptor defect Vitamin b deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CD320(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 106 →
methylmalonic acidemia with homocystinuria, type cblJ Vitamin b deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCD4(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency Vitamin b deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMUT(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Megaloblastic anemia methylmalonic aciduria, cblA type
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMAA(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 106 →
methylmalonic aciduria, cblA type Vitamin b deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMAA(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 106 →
Methylmalonyl-coa mutase deficiency Vitamin b deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMUT(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Lennox-gastaut syndrome Mowat-wilson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZEB2(7)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Intestinal neoplasms multiple endocrine neoplasia type 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDKN1B(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Frontotemporal dementia with or without amyotrophic lateral sclerosis Multiple familial trichoepithelioma
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYLD(6)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
myasthenic syndrome, congenital, 1b, fast-channel Postsynaptic congenital myasthenic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHRNA1(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 34 →
Developmental coordination disorder PTEN hamartoma tumor syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTEN(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Developmental coordination disorder frontotemporal dementia and/or amyotrophic lateral sclerosis 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
SQSTM1(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
amyotrophic lateral sclerosis type 1 Developmental coordination disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOD1(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Ankylosis Developmental coordination disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(2)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Developmental delay with autism spectrum disorder Eye neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
HERC2(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Developmental delay with behavioral abnormalities Specific learning disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADGRL1(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 268 →
dilated cardiomyopathy 1C Myofibrillar myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
LDB3(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —

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