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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
Psoriasis Worster drought syndrome
1 gene
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1 of 1 corroborated by 2+ sources
TMTC4(2)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
intellectual disability, autosomal recessive 61 Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
RUSC2(2)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
Ditra syndrome Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
IL36RN(6)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
autosomal recessive cerebellar ataxia Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
CWF19L1(2)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
autosomal recessive osteopetrosis 5 Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
OSTM1(2)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
BBS7-related ciliopathy Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
BBS7(2)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. —
Benign flecked retina Psoriasis
1 gene
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1 of 1 corroborated by 2+ sources
PLA2G5(3)
0.001 1.000 4.75e-2 4.92e-2 ✓ sig. Cluster 28 →
autosomal recessive spinocerebellar ataxia 14 Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
SPTBN2(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
POU3F3(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic skeletal Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(4)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic speech skeletal Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
12q15q21 microdeletion syndrome Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
CNOT2(3)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
ALG12-congenital disorder of glycosylation Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
ALG12(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Osteoarthritis tooth agenesis, selective, 3
1 gene
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1 of 1 corroborated by 2+ sources
PAX9(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Osteoarthritis Zaki syndrome
1 gene
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1 of 1 corroborated by 2+ sources
WLS(3)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
long chain 3-hydroxyacyl-coa dehydrogenase deficiency Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
HADHA(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
ciliary dyskinesia, primary, 54 Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
CFAP54(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Citrin deficiency Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
COG5-congenital disorder of glycosylation Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
COG5(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Congenital lactase deficiency Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
LCT(4)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. Cluster 2 →
congenital myasthenic syndrome 12 Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
GFPT1(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Congenital right-sided heart lesions Osteoarthritis
1 gene
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SLC27A6(1)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Craniolenticulosutural dysplasia Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
SEC23A(6)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. Cluster 2 →
Delayed sleep phase syndrome Osteoarthritis
1 gene
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1 of 1 corroborated by 2+ sources
CRY1(3)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —
Osteoarthritis Pemphigus foliaceus
1 gene
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1 of 1 corroborated by 2+ sources
RAN(2)
0.001 1.000 4.74e-2 4.92e-2 ✓ sig. —

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