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
Cannabis abuse short chain acyl-coa dehydrogenase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACADS(2)
0.009 1.000 7.53e-3 8.83e-3 ✓ sig. —
Cannabis abuse Dorfman-chanarin disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABHD5(3)
0.009 1.000 7.53e-3 8.83e-3 ✓ sig. —
Cannabis abuse Cohen-gibson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EED(6)
0.009 1.000 7.53e-3 8.83e-3 ✓ sig. —
Carpenter syndrome Polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
MEGF8(3)
0.024 0.333 7.58e-3 8.88e-3 ✓ sig. —
3mc syndrome Nasal polyp
1 gene
Show details
COLEC10(1)
0.024 0.333 7.58e-3 8.88e-3 ✓ sig. —
Malpuech facial clefting syndrome Nasal polyp
1 gene
Show details
1 of 1 corroborated by 2+ sources
COLEC10(3)
0.024 0.333 7.58e-3 8.88e-3 ✓ sig. —
Connective tissue disease mend syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EBP(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
multiple endocrine neoplasia type 1 Pancreatic neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
MEN1(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease Multiple epiphyseal dysplasia with early-onset diabetes mellitus
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF2AK3(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Brachytelephalangic chondrodysplasia punctata Connective tissue disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ARSL(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Camptodactyly Pancreatic neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
TLN2(3)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease neurodevelopmental disorder with microcephaly and dysmorphic facies
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPOP(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPOP(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease TRIP11-related skeletal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIP11(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease Warburg-cinotti syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DDR2(5)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease Wolcott-rallison syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF2AK3(4)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease X-linked dominant chondrodysplasia punctata
1 gene
Show details
1 of 1 corroborated by 2+ sources
EBP(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Comp-related skeletal dysplasia Connective tissue disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
COMP(3)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Congenital tufting enteropathy Pancreatic neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPCAM(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Anovulation Pancreatic neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR5A2(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease schneckenbecken dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC35D1(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. Cluster 12 →
Connective tissue disease short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC10A7(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DDR2(2)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Connective tissue disease Dyggve-melchior-clausen syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYM(5)
0.008 1.000 7.60e-3 8.90e-3 ✓ sig. —
Craniosynostosis Developmental delay with variable intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCF20(5)
0.016 0.500 7.65e-3 8.95e-3 ✓ sig. —

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