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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 1 Thoracic malformation
1 gene
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1 of 1 corroborated by 2+ sources
FGF4(3)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 hyperphosphatasia with intellectual disability syndrome 4
1 gene
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1 of 1 corroborated by 2+ sources
PGAP3(2)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 MAN1B1-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
MAN1B1(2)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 maturity-onset diabetes of the young type 8
1 gene
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1 of 1 corroborated by 2+ sources
CEL(3)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 Mineralocortocoid excess
1 gene
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1 of 1 corroborated by 2+ sources
HSD11B2(7)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 Intellectual developmental disorder neuropsychiatric
1 gene
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1 of 1 corroborated by 2+ sources
SLC45A1(4)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 Pemphigus foliaceus
1 gene
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1 of 1 corroborated by 2+ sources
RAN(2)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Diabetes mellitus type 1 PGM1-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
PGM1(2)
0.002 1.000 3.10e-2 3.29e-2 ✓ sig. —
Heart failure PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
1 gene
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1 of 1 corroborated by 2+ sources
PHIP(2)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Heart failure phosphoenolpyruvate carboxykinase deficiency, cytosolic
1 gene
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1 of 1 corroborated by 2+ sources
PCK1(3)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Heart failure pseudohypoaldosteronism type 2D
1 gene
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1 of 1 corroborated by 2+ sources
KLHL3(2)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Developmental delay with intellectual disability and obesity Heart failure
1 gene
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1 of 1 corroborated by 2+ sources
PHIP(2)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Heart failure Hmg-coa synthase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
HMGCS2(4)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Heart failure Yoon-bellen neurodevelopmental syndrome
1 gene
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1 of 1 corroborated by 2+ sources
OGDHL(4)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Congenital right-sided heart lesions Heart failure
1 gene
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SLC27A6(1)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
fontaine progeroid syndrome Heart failure
1 gene
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1 of 1 corroborated by 2+ sources
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Acetyl-coa carboxylase deficiency Heart failure
1 gene
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1 of 1 corroborated by 2+ sources
ACACA(3)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
Chung-jansen syndrome Heart failure
1 gene
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1 of 1 corroborated by 2+ sources
PHIP(2)
0.002 1.000 3.05e-2 3.24e-2 ✓ sig. —
ciliary dyskinesia, primary, 42 Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
MCIDAS(2)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
ciliary dyskinesia, primary, 53 Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
CLXN(2)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
maternal riboflavin deficiency Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
SLC52A1(2)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
12q15q21 microdeletion syndrome Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(3)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic skeletal Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(4)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic speech skeletal Ovarian cancer
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(2)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —
BARD1-related cancer predisposition Ovarian cancer
1 gene
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BARD1(1)
0.002 1.000 3.03e-2 3.21e-2 ✓ sig. —

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