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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
Desbuquois syndrome meier-gorlin syndrome 3
1 gene
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1 of 1 corroborated by 2+ sources
ORC6(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome meier-gorlin syndrome 4
1 gene
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1 of 1 corroborated by 2+ sources
CDT1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome meier-gorlin syndrome 5
1 gene
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1 of 1 corroborated by 2+ sources
CDC6(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome meier-gorlin syndrome 6
1 gene
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1 of 1 corroborated by 2+ sources
GMNN(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome meier-gorlin syndrome 7
1 gene
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1 of 1 corroborated by 2+ sources
CDC45(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mend syndrome
1 gene
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1 of 1 corroborated by 2+ sources
EBP(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome microcephalic osteodysplastic dysplasia, Saul-Wilson type
1 gene
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1 of 1 corroborated by 2+ sources
COG4(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome microcephaly with or without short stature
1 gene
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1 of 1 corroborated by 2+ sources
CEP152(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome
1 gene
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1 of 1 corroborated by 2+ sources
AMMECR1(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis type 3C
1 gene
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1 of 1 corroborated by 2+ sources
HGSNAT(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis type 3D
1 gene
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1 of 1 corroborated by 2+ sources
GNS(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis type 4A
1 gene
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1 of 1 corroborated by 2+ sources
GALNS(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis type 6
1 gene
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1 of 1 corroborated by 2+ sources
ARSB(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis type 7
1 gene
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1 of 1 corroborated by 2+ sources
GUSB(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome mucopolysaccharidosis-plus syndrome
1 gene
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1 of 1 corroborated by 2+ sources
VPS33A(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome netherton syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SPINK5(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities
1 gene
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1 of 1 corroborated by 2+ sources
PPP1R21(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. Cluster 68 →
Desbuquois syndrome opsismodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
INPPL1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Osteocraniostenosis
1 gene
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1 of 1 corroborated by 2+ sources
FAM111A(4)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Desmosterolosis
1 gene
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1 of 1 corroborated by 2+ sources
DHCR24(7)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Diaphanospondylodysostosis
1 gene
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1 of 1 corroborated by 2+ sources
BMPER(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Doughnut lesion of calvaria and bone fragility syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SGMS2(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome ehlers-danlos syndrome, musculocontractural type 2
1 gene
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1 of 1 corroborated by 2+ sources
DSE(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Enteropathy
1 gene
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1 of 1 corroborated by 2+ sources
SLCO2A1(3)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome FAM111A-related skeletal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
FAM111A(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —

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