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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.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Congenital nasopharyngeal atresia primary ciliary dyskinesia 16
1 gene
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1 of 1 corroborated by 2+ sources
DNAL1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 17
1 gene
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1 of 1 corroborated by 2+ sources
DNAAF19(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 18
1 gene
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1 of 1 corroborated by 2+ sources
DNAAF5(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 19
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAAF11(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital nasopharyngeal atresia primary ciliary dyskinesia 2
1 gene
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1 of 1 corroborated by 2+ sources
DNAAF3(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 20
1 gene
Show details
1 of 1 corroborated by 2+ sources
ODAD1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital nasopharyngeal atresia primary ciliary dyskinesia 21
1 gene
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1 of 1 corroborated by 2+ sources
DRC1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 22
1 gene
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1 of 1 corroborated by 2+ sources
ZMYND10(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 23
1 gene
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1 of 1 corroborated by 2+ sources
ODAD2(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 24
1 gene
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1 of 1 corroborated by 2+ sources
RSPH1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 25
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAAF4(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 26
1 gene
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1 of 1 corroborated by 2+ sources
CFAP298(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital nasopharyngeal atresia primary ciliary dyskinesia 28
1 gene
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1 of 1 corroborated by 2+ sources
SPAG1(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital nasopharyngeal atresia primary ciliary dyskinesia 29
1 gene
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1 of 1 corroborated by 2+ sources
CCNO(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 3
1 gene
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1 of 1 corroborated by 2+ sources
DNAH5(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 30
1 gene
Show details
1 of 1 corroborated by 2+ sources
ODAD3(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 32
1 gene
Show details
1 of 1 corroborated by 2+ sources
RSPH3(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 5
1 gene
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1 of 1 corroborated by 2+ sources
HYDIN(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital nasopharyngeal atresia primary ciliary dyskinesia 7
1 gene
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1 of 1 corroborated by 2+ sources
DNAH11(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital nasopharyngeal atresia primary ciliary dyskinesia 9
1 gene
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1 of 1 corroborated by 2+ sources
DNAI2(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. Cluster 9 →
Congenital cartilage disorder radioulnar synostosis with amegakaryocytic thrombocytopenia 1
1 gene
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1 of 1 corroborated by 2+ sources
HOXA11(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Developmental delay with or without epilepsy West syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SPTAN1(3)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Dna ligase iv deficiency Spondylosis
1 gene
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1 of 1 corroborated by 2+ sources
LIG4(4)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Congenital cartilage disorder Dyggve-melchior-clausen syndrome
1 gene
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1 of 1 corroborated by 2+ sources
DYM(5)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —
Early-onset obesity-hyperphagia-severe developmental delay syndrome West syndrome
1 gene
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1 of 1 corroborated by 2+ sources
NTRK2(2)
0.032 1.000 1.95e-3 2.83e-3 ✓ sig. —

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