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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
Macular degeneration Schmid metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL10A1(2)
0.015 1.000 4.35e-3 5.46e-3 ✓ sig. —
Metaphyseal chondrodysplasia with retinitis pigmentosa Urinary bladder cancer
1 gene
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1 of 1 corroborated by 2+ sources
CWC27(5)
0.015 1.000 4.29e-3 5.38e-3 ✓ sig. —
Carpal tunnel syndrome Schmid metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL10A1(2)
0.016 1.000 4.09e-3 5.16e-3 ✓ sig. —
Metaphyseal chondrodysplasia with retinitis pigmentosa Osteonecrosis
1 gene
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1 of 1 corroborated by 2+ sources
CWC27(5)
0.025 1.000 2.53e-3 3.45e-3 ✓ sig. Cluster 373 →
Osteochondrodysplasias Schmid metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL10A1(2)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Congenital cartilage disorder Schmid metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL10A1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Diverticulitis Metaphyseal chondrodysplasia with retinitis pigmentosa
1 gene
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1 of 1 corroborated by 2+ sources
CWC27(5)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. Cluster 373 →
Metaphyseal chondrodysplasia Trichorhinophalangeal syndrome
1 gene
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1 of 1 corroborated by 2+ sources
TRPS1(7)
0.091 0.333 1.56e-3 2.38e-3 ✓ sig. —
Metaphyseal chondrodysplasia Metaphyseal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
MMP13(6)
0.091 0.333 1.56e-3 2.38e-3 ✓ sig. —
Metaphyseal chondrodysplasia Metaphyseal enchondromatosis
1 gene
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1 of 1 corroborated by 2+ sources
IDH1(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Coronary artery dissection Metaphyseal chondrodysplasia
1 gene
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FBN1(1)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Congenital pectus carinatum Metaphyseal chondrodysplasia
1 gene
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FBN1(1)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
COL10A1(6)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Metaphyseal chondrodysplasia SF3B4-related acrofacial dysostosis
1 gene
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1 of 1 corroborated by 2+ sources
SF3B4(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Eiken skeletal dysplasia Metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
PTH1R(6)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Blomstrand lethal chondrodysplasia Metaphyseal chondrodysplasia
1 gene
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1 of 1 corroborated by 2+ sources
PTH1R(4)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Aneurysm Metaphyseal chondrodysplasia
2 genes
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2 of 2 corroborated by 2+ sources
FBN1(2), MMP13(5)
0.059 0.250 8.24e-5 2.94e-4 ✓ sig. —
Metaphyseal chondrodysplasia with retinitis pigmentosa Retinitis pigmentosa with or without skeletal anomalies
1 gene
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1 of 1 corroborated by 2+ sources
CWC27(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 373 →
Brachydactyly-short stature-retinits pigmentosa syndrome Metaphyseal chondrodysplasia with retinitis pigmentosa
1 gene
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1 of 1 corroborated by 2+ sources
CWC27(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 373 →

Showing 19 of 19 matching pairs, sorted by significance (descending). Click a column header to sort.