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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
Biliary atresia Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome
1 gene
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1 of 1 corroborated by 2+ sources
GLIS3(3)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome Primary angle closure glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
GLIS3(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Angle closure glaucoma Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome
1 gene
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1 of 1 corroborated by 2+ sources
GLIS3(2)
0.067 1.000 9.09e-4 1.58e-3 ✓ sig. —
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome Periprosthetic osteolysis
1 gene
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1 of 1 corroborated by 2+ sources
GLIS3(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. Cluster 394 →
Congenital keratoglobus Primary congenital glaucoma
1 gene
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LTBP2(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Congenital glaucoma CYP1B1-related glaucoma with or without anterior segment dysgenesis
1 gene
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1 of 1 corroborated by 2+ sources
CYP1B1(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Bockenheimer syndrome Congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
TEK(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital glaucoma Mucocutaneous venous malformations
1 gene
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1 of 1 corroborated by 2+ sources
TEK(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
glaucoma 3, primary congenital, d Primary congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
LTBP2(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. —
Mucocutaneous venous malformations Primary congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
TEK(3)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. —
Bockenheimer syndrome Primary congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
TEK(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. —
Microspherophakia Primary congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
LTBP2(5)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. —
CYP1B1-related glaucoma with or without anterior segment dysgenesis Primary congenital glaucoma
1 gene
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1 of 1 corroborated by 2+ sources
CYP1B1(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. —
Neonatal diabetes mellitus with congenital hypothyroidism Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome
1 gene
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1 of 1 corroborated by 2+ sources
GLIS3(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 394 →
Congenital glaucoma Primary congenital glaucoma
3 genes
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3 of 3 corroborated by 2+ sources
CYP1B1(2), TEK(4), LTBP2(3)
0.333 0.750 2.30e-10 2.21e-9 ✓ sig. —
Hydrophthalmos Primary congenital glaucoma
3 genes
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1 of 3 corroborated by 2+ sources
CYP1B1(1), TEK(2), LTBP2(1)
0.375 0.750 1.31e-10 1.29e-9 ✓ sig. —
Congenital glaucoma Hydrophthalmos
6 genes
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6 of 6 corroborated by 2+ sources
TCF7L2(2), CYP1B1(2), TEK(3), MYOC(3), GPATCH3(2), LTBP2(3)
0.750 1.000 3.79e-22 7.87e-21 ✓ sig. —

Showing 17 of 17 matching pairs, sorted by significance (descending). Click a column header to sort.