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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 Familial telangiectasia cancer syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ATR(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome fatty acyl-CoA reductase 1 deficiency
1 gene
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1 of 1 corroborated by 2+ sources
FAR1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome fatty acyl-CoA reductase 1 upregulation
1 gene
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1 of 1 corroborated by 2+ sources
FAR1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome fontaine progeroid syndrome
1 gene
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1 of 1 corroborated by 2+ sources
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ALX1(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome frontorhiny
1 gene
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1 of 1 corroborated by 2+ sources
ALX3(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome fucosidosis
1 gene
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1 of 1 corroborated by 2+ sources
FUCA1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome glyceronephosphate O-acyltransferase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
GNPAT(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome GNPTAB-mucolipidosis
1 gene
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1 of 1 corroborated by 2+ sources
GNPTAB(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome GNPTG-mucolipidosis
1 gene
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1 of 1 corroborated by 2+ sources
GNPTG(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Gollop-wolfgang complex
1 gene
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1 of 1 corroborated by 2+ sources
BHLHA9(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome GPR161-related medulloblastoma predisposition
1 gene
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1 of 1 corroborated by 2+ sources
GPR161(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Parathyroid carcinoma
1 gene
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1 of 1 corroborated by 2+ sources
CDC73(4)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Parathyroid neoplasm
1 gene
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1 of 1 corroborated by 2+ sources
CDC73(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Peroxisomal fatty acyl-coa reductase 1 disorder
1 gene
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1 of 1 corroborated by 2+ sources
FAR1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome Postaxial acrofacial dysostosis
1 gene
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1 of 1 corroborated by 2+ sources
DHODH(4)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome pycnodysostosis
1 gene
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1 of 1 corroborated by 2+ sources
CTSK(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome RAB23-related Carpenter syndrome
1 gene
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1 of 1 corroborated by 2+ sources
RAB23(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Multiple sclerosis RCBTB1-related retinopathy
1 gene
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1 of 1 corroborated by 2+ sources
RCBTB1(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis X-linked epilepsy with or without intellectual disability and dysmorphic features
1 gene
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1 of 1 corroborated by 2+ sources
GABRA3(4)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
Multiple sclerosis Ziegler-huang syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SLC30A7(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
C syndrome Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
CD96(6)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
congenital disorder of glycosylation with defective fucosylation 1 Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
FUT8(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
immunodeficiency 106, susceptibility to viral infections Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
IFNAR1(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —
inflammatory bowel disease 25 Multiple sclerosis
1 gene
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1 of 1 corroborated by 2+ sources
IL10RB(2)
0.002 1.000 3.74e-2 3.93e-2 ✓ sig. —

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