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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
Apolipoprotein c-ii deficiency Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
APOC2(5)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Baralle-macken syndrome Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
COPB1(4)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis RFT1-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
RFT1(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis seizures, early-onset, with neurodegeneration and brain calcifications
1 gene
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1 of 1 corroborated by 2+ sources
NRROS(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis Telangiectasia–intellectual disability–microcephaly–metaphyseal dysplasia–eye abnormalities–short stature syndrome
1 gene
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1 of 1 corroborated by 2+ sources
LRRC8C(4)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
leukodystrophy, hypomyelinating, 22 Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
CLDN11(3)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
LZTFL1-related ciliopathy Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
LZTFL1(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis NIK deficiency
1 gene
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1 of 1 corroborated by 2+ sources
MAP3K14(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Childhood kidney wilms tumor Colorectal neoplasms
1 gene
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1 of 1 corroborated by 2+ sources
TRIM28(2)
0.003 0.500 3.74e-2 3.93e-2 ✓ sig. —
Bloom syndrome Colorectal neoplasms
1 gene
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1 of 1 corroborated by 2+ sources
UNG(2)
0.003 0.500 3.74e-2 3.93e-2 ✓ sig. —
immunodeficiency 76 Myocardial infarction
1 gene
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1 of 1 corroborated by 2+ sources
FCHO1(2)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Myocardial infarction Woolly hair-skin fragility syndrome
1 gene
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1 of 1 corroborated by 2+ sources
TUFT1(4)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Myocardial infarction Xia-gibbs syndrome
1 gene
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1 of 1 corroborated by 2+ sources
AHDC1(3)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Congenital right-sided heart lesions Myocardial infarction
1 gene
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SLC27A6(1)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Mineralocortocoid excess Myocardial infarction
1 gene
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1 of 1 corroborated by 2+ sources
HSD11B2(7)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Myocardial infarction
1 gene
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1 of 1 corroborated by 2+ sources
AHDC1(2)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Myocardial infarction Richieri costa pereira syndrome
1 gene
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1 of 1 corroborated by 2+ sources
EIF4A3(5)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Myocardial infarction Robin sequence with cleft mandible and limb anomalies
1 gene
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1 of 1 corroborated by 2+ sources
EIF4A3(2)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Beta-ureidopropionase deficiency Myocardial infarction
1 gene
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1 of 1 corroborated by 2+ sources
UPB1(7)
0.002 1.000 3.77e-2 3.95e-2 ✓ sig. —
Diabetes mellitus Tropical calcific pancreatitis
1 gene
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1 of 1 corroborated by 2+ sources
SPINK1(5)
0.003 0.500 3.81e-2 3.99e-2 ✓ sig. —
Congenital chronic diarrhea with protein-losing enteropathy Diabetes mellitus
1 gene
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1 of 1 corroborated by 2+ sources
DGAT1(3)
0.003 0.500 3.81e-2 3.99e-2 ✓ sig. —
Dementia Webb-dattani syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ARNT2(5)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
C syndrome Dementia
1 gene
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1 of 1 corroborated by 2+ sources
CD96(7)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia polyglucosan body myopathy type 2
1 gene
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1 of 1 corroborated by 2+ sources
GYG1(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia primary ciliary dyskinesia 9
1 gene
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1 of 1 corroborated by 2+ sources
DNAI2(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —

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