Shared-Gene Disease Pairs?
Disease pairs ranked by curated gene overlap — a data-driven way to spot diseases that aren't normally considered related but share a large number of underlying genes. Looking for groups of more than two? See Disease Clusters.
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.
| Disease A ⇵ | Disease B ⇵ | Shared genes ⇵ | Similarity score ⇵ | Overlap coefficient ⇵ | P-value ⇵ | FDR q-value ▲ | Shared cluster | |
|---|---|---|---|---|---|---|---|---|
| Multinodular goiter | Toxic nodular goiter |
10 genes
|
0.278 | 0.588 | 1.23e-24 | 3.10e-23 ✓ sig. | — | |
| Hyperthyroidism | Multinodular goiter |
6 genes
|
0.079 | 0.214 | 4.41e-10 | 4.38e-9 ✓ sig. | — | |
| Multinodular goiter | Thyroid disease |
5 genes
|
0.065 | 0.179 | 3.69e-8 | 2.92e-7 ✓ sig. | — | |
| Multinodular goiter | Urinary system disease |
2 genes
|
0.048 | 0.133 | 3.30e-4 | 7.70e-4 ✓ sig. | — | |
| 1p31p32 microdeletion syndrome | Multinodular goiter |
1 gene
|
0.034 | 1.000 | 1.82e-3 | 2.66e-3 ✓ sig. | — | |
| Multinodular goiter | progressive encephalopathy with leukodystrophy due to DECR deficiency |
1 gene
|
0.034 | 1.000 | 1.82e-3 | 2.66e-3 ✓ sig. | — | |
| 2,4-dienoyl-coa reductase deficiency | Multinodular goiter |
1 gene
|
0.033 | 0.500 | 3.63e-3 | 4.66e-3 ✓ sig. | — | |
| Multinodular goiter | Ochoa syndrome |
1 gene
|
0.033 | 0.500 | 3.63e-3 | 4.66e-3 ✓ sig. | — | |
| Multinodular goiter | Urofacial syndrome |
1 gene
|
0.033 | 0.500 | 3.63e-3 | 4.66e-3 ✓ sig. | — |
0 selected
·
Loading clusters...
Showing 9 of 9 matching pairs, sorted by significance (ascending). Click a column header to sort.