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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
Coasy protein-associated neurodegeneration Coenzyme a synthase protein associated neurodegeneration
1 gene
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1 of 1 corroborated by 2+ sources
COASY(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Coats disease norrie disease
1 gene
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1 of 1 corroborated by 2+ sources
NDP(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Cobalamin metabolism disorder inborn disorder of cobalamin metabolism and transport
1 gene
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1 of 1 corroborated by 2+ sources
MMADHC(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Cocoon syndrome Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiency
1 gene
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1 of 1 corroborated by 2+ sources
CHUK(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COG4-congenital disorder of glycosylation Saul-wilson syndrome
1 gene
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1 of 1 corroborated by 2+ sources
COG4(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COG4-congenital disorder of glycosylation microcephalic osteodysplastic dysplasia, Saul-Wilson type
1 gene
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COG4(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COL1A1-related Ehlers-Danlos syndrome Maternal hypertension
1 gene
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1 of 1 corroborated by 2+ sources
COL1A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 138 →
COL1A1-related Ehlers-Danlos syndrome Rhizomelia
1 gene
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1 of 1 corroborated by 2+ sources
COL1A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 138 →
COL1A2-related Ehlers-Danlos syndrome ehlers-danlos syndrome, cardiac valvular type
1 gene
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COL1A2(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COL1A2-related Ehlers-Danlos syndrome COL1A2-related osteogenesis imperfecta
1 gene
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COL1A2(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COL1A2-related osteogenesis imperfecta ehlers-danlos syndrome, cardiac valvular type
1 gene
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COL1A2(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
COL2A1-related spondyloepiphyseal dysplasia Collagenopathy
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
COL2A1-related spondyloepiphyseal dysplasia Coxa plana
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
COL2A1-related spondyloepiphyseal dysplasia Czech dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
COL2A1-related spondyloepiphyseal dysplasia Dysspondyloenchondromatosis
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
COL2A1-related spondyloepiphyseal dysplasia kniest dysplasia
1 gene
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COL2A1(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
COL4A1-related disorder Familial hematuria-retinal arteriolar tortuosity-contractures syndrome
1 gene
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1 of 1 corroborated by 2+ sources
COL4A1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 154 →
COL4A1-related disorder Colpocephaly
1 gene
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1 of 1 corroborated by 2+ sources
COL4A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 154 →
COL4A1-related disorder Retinal arterial tortuosity
1 gene
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1 of 1 corroborated by 2+ sources
COL4A1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 154 →
Cole disease Coronary medial sclerosis of infancy
1 gene
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1 of 1 corroborated by 2+ sources
ENPP1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 128 →
Cole disease hypopigmentation-punctate palmoplantar keratoderma syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ENPP1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 128 →
Collagenopathy Coxa plana
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
Collagenopathy Czech dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
Collagenopathy Dysspondyloenchondromatosis
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →
Collagenopathy kniest dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL2A1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 11 →

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