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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
Diabetes mellitus type 2 immunodeficiency, common variable, 7
1 gene
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1 of 1 corroborated by 2+ sources
CR2(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 inflammatory skin and bowel disease, neonatal, 1
1 gene
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1 of 1 corroborated by 2+ sources
ADAM17(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Insulinomatosis and diabetes mellitus
1 gene
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1 of 1 corroborated by 2+ sources
MAFA(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Intellectual developmental disorder dysmorphic strabismus
1 gene
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1 of 1 corroborated by 2+ sources
ADAT3(5)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Nasopalpebral lipoma-coloboma syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ZDBF2(3)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 nephronophthisis 20
1 gene
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1 of 1 corroborated by 2+ sources
MAPKBP1(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 nephronophthisis 7
1 gene
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1 of 1 corroborated by 2+ sources
GLIS2(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 non-severe combined immunodeficiency due to COPG1 deficiency
1 gene
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1 of 1 corroborated by 2+ sources
COPG1(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Oculocerebrodental syndrome
1 gene
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1 of 1 corroborated by 2+ sources
PIK3C2A(3)
0.000 1.000 2.00e-1 2.00e-1 Cluster 2 →
Diabetes mellitus type 2 opsismodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
INPPL1(3)
0.000 1.000 2.00e-1 2.00e-1 Cluster 2 →
Diabetes mellitus type 2 hemochromatosis type 2A
1 gene
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1 of 1 corroborated by 2+ sources
HJV(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Hepatic glycogen synthase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
GYS2(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 hyper-IgE recurrent infection syndrome 3, autosomal recessive
1 gene
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1 of 1 corroborated by 2+ sources
ZNF341(2)
0.000 1.000 2.00e-1 2.00e-1 —
Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus Diabetes mellitus type 2
1 gene
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1 of 1 corroborated by 2+ sources
DNAJC3(4)
0.000 1.000 2.00e-1 2.00e-1 —
Autoinflammatory disease, multisystem, with immune dysregulation, x-linked Diabetes mellitus type 2
1 gene
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1 of 1 corroborated by 2+ sources
DOCK11(6)
0.000 1.000 2.00e-1 2.00e-1 —
Autoinflammatory disease, systemic, with vasculitis Diabetes mellitus type 2
1 gene
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1 of 1 corroborated by 2+ sources
LYN(4)
0.000 1.000 2.00e-1 2.00e-1 —
Bilateral cleft lip Diabetes mellitus type 2
1 gene
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1 of 1 corroborated by 2+ sources
PLEKHA5(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 lysinuric protein intolerance
1 gene
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1 of 1 corroborated by 2+ sources
SLC7A7(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Midline facial cleft
1 gene
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1 of 1 corroborated by 2+ sources
PCSK7(2)
0.000 1.000 2.00e-1 2.00e-1 —
Developmental delay with variable neurological abnormalities Diabetes mellitus type 2
1 gene
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1 of 1 corroborated by 2+ sources
LMBRD2(5)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Dihydropyrimidinase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
DPYS(5)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Dimethylglycine dehydrogenase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
DMGDH(7)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Early-onset immune dysregulation due to dock11 complete deficiency
1 gene
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1 of 1 corroborated by 2+ sources
DOCK11(3)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Early-onset immune dysregulation with autoimmunity due to dock11 partial deficiency
1 gene
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1 of 1 corroborated by 2+ sources
DOCK11(3)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 El-hayek-chahrour neurodevelopmental syndrome
1 gene
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1 of 1 corroborated by 2+ sources
KDM5A(5)
0.000 1.000 2.00e-1 2.00e-1 —

Showing 25 of 20825 pairs, sorted by significance (ascending). Click a column header to sort.