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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.
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Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Cerebral amyloid angiopathy Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
1 gene
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1 of 1 corroborated by 2+ sources
0.014 0.500 9.20e-3 1.05e-2 ✓ sig. —
Abri amyloidosis Cerebral amyloid angiopathy
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(3)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy Uridine-cytidineuria
1 gene
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1 of 1 corroborated by 2+ sources
SLC28A1(3)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy
1 gene
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1 of 1 corroborated by 2+ sources
CST3(3)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy immunodeficiency 53
1 gene
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1 of 1 corroborated by 2+ sources
RELB(2)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy immunodeficiency 122
1 gene
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1 of 1 corroborated by 2+ sources
POLD3(2)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy Familial danish dementia
1 gene
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1 of 1 corroborated by 2+ sources
ITM2B(3)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Acys amyloidosis Cerebral amyloid angiopathy
1 gene
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1 of 1 corroborated by 2+ sources
CST3(4)
0.014 1.000 4.61e-3 5.73e-3 ✓ sig. —
Cerebral amyloid angiopathy Vascular dementia
5 genes
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3 of 5 corroborated by 2+ sources
APP(6), ITM2B(3), APOE(3), GRIK2(1), PRNP(1)
0.026 0.070 3.08e-4 7.71e-4 ✓ sig. —
Amyloid neuropathy cerebral amyloid angiopathy, app-related
1 gene
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1 of 1 corroborated by 2+ sources
APP(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 116 →
Cerebral amyloid angiopathy Conduct disorder
4 genes
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PTPRD(1), SLC7A2(1), ADH1B(1), ADH1C(1)
0.033 0.077 9.51e-5 3.38e-4 ✓ sig. —
cerebral amyloid angiopathy, app-related Partial epilepsy with variable foci
1 gene
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1 of 1 corroborated by 2+ sources
APP(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 116 →
cerebral amyloid angiopathy, app-related Eye manifestations
1 gene
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1 of 1 corroborated by 2+ sources
APP(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 116 →
Amyloid angiopathy cerebral amyloid angiopathy, app-related
1 gene
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1 of 1 corroborated by 2+ sources
APP(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 116 →
Abeta amyloidosis cerebral amyloid angiopathy, app-related
1 gene
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1 of 1 corroborated by 2+ sources
APP(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 116 →
Cerebral amyloid angiopathy Dementia
22 genes
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4 of 22 corroborated by 2+ sources
APP(6), ITM2B(3), APOE(3), DOCK10(1), EFHB(1), FSTL5(1), GRIK2(1), KAZN(1), KCNH8(1), NCK2(1), NECTIN2(1), PTPRD(1) +10 more
0.034 0.310 9.96e-15 1.40e-13 ✓ sig. —
Cerebral amyloid angiopathy Lewy body disease
13 genes
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1 of 13 corroborated by 2+ sources
APOC1(1), APOE(3), CDKAL1(1), KAZN(1), PTPRD(1), SGK1(1), HS3ST4(1), ATP10A(1), POLD3(1), ABTB2(1), KCNB2(1), RAG1(1) +1 more
0.084 0.183 3.48e-16 5.37e-15 ✓ sig. —
Brain infarction Cerebral amyloid angiopathy
12 genes
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1 of 12 corroborated by 2+ sources
APOE(3), CDKAL1(1), KAZN(1), PTPRD(1), SGK1(1), HS3ST4(1), ATP10A(1), POLD3(1), ABTB2(1), KCNB2(1), RAG1(1), SLC29A4(1)
0.125 0.333 3.99e-20 7.65e-19 ✓ sig. —

Showing 18 of 18 matching pairs, sorted by significance (descending). Click a column header to sort.