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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 Thoracic malformation
1 gene
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1 of 1 corroborated by 2+ sources
FGF4(3)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 VPS11-related neurological disorder
1 gene
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1 of 1 corroborated by 2+ sources
VPS11(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 Warsaw breakage syndrome
1 gene
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1 of 1 corroborated by 2+ sources
DDX11(7)
0.000 1.000 2.00e-1 2.00e-1 Cluster 2 →
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 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 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 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 fanconi anemia complementation group p
1 gene
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1 of 1 corroborated by 2+ sources
SLX4(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 GNPTG-mucolipidosis
1 gene
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1 of 1 corroborated by 2+ sources
GNPTG(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 glycogen storage disorder due to 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 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 —
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 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 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 —
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 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 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 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 SNUPN-related muscular dystrophy with or without multi-system involvement
1 gene
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1 of 1 corroborated by 2+ sources
SNUPN(2)
0.000 1.000 2.00e-1 2.00e-1 Cluster 2 →
Diabetes mellitus type 2 siddiqi syndrome
1 gene
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1 of 1 corroborated by 2+ sources
FITM2(2)
0.000 1.000 2.00e-1 2.00e-1 Cluster 2 →
Diabetes mellitus type 2 syndactyly-telecanthus-anogenital and renal malformations syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CCNQ(2)
0.000 1.000 2.00e-1 2.00e-1 —
Diabetes mellitus type 2 renal hypomagnesemia 2
1 gene
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1 of 1 corroborated by 2+ sources
FXYD2(2)
0.000 1.000 2.00e-1 2.00e-1 —

Showing 25 of 20918 pairs, sorted by significance (descending). Click a column header to sort.