Log in to save this analysis

Save This Analysis

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.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▲ Shared cluster
Coenzyme q10 deficiency Primary coenzyme q10 deficiency
2 genes
Show details
2 of 2 corroborated by 2+ sources
COQ6(5), COQ7(5)
0.154 1.000 5.57e-7 3.41e-6 ✓ sig. —
Coq7-related distal hereditary motor neuropathy Primary coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ7(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Ataxia with oculomotor apraxia and hypoalbuminemia Coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
APTX(3)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Coenzyme q10 deficiency Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PDSS1(5)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Coenzyme q10 deficiency Coq7-related distal hereditary motor neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ7(4)
0.077 1.000 7.79e-4 1.41e-3 ✓ sig. —
Coenzyme q10 deficiency Shy-drager syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ2(4)
0.067 0.333 2.34e-3 3.24e-3 ✓ sig. —
Autosomal recessive ataxia Coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ8A(7)
0.059 0.200 3.89e-3 4.94e-3 ✓ sig. —
Distal hereditary motor neuropathy Primary coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ7(5)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Alzheimer disease Primary coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ6(2)
0.000 0.500 2.67e-1 2.68e-1 —

Showing 9 of 9 matching pairs, sorted by significance (ascending). Click a column header to sort.