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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
Intellectual developmental disorder Intellectual developmental disorder, autosomal dominant 57
1 gene
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1 of 1 corroborated by 2+ sources
TLK2(5)
0.001 1.000 5.26e-2 5.42e-2 —
Intellectual developmental disorder, autosomal dominant 51 Non-specific syndromic intellectual disability
1 gene
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1 of 1 corroborated by 2+ sources
KMT5B(2)
0.003 1.000 2.38e-2 2.53e-2 ✓ sig. —
Congenital heart disease Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities
1 gene
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NAA15(1)
0.006 1.000 1.15e-2 1.27e-2 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 52 Liver neoplasms
1 gene
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1 of 1 corroborated by 2+ sources
ASH1L(2)
0.007 1.000 9.62e-3 1.08e-2 ✓ sig. —
Developmental disability Intellectual developmental disorder, autosomal dominant 57
1 gene
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1 of 1 corroborated by 2+ sources
TLK2(2)
0.007 1.000 9.23e-3 1.04e-2 ✓ sig. —
Developmental disability Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities
1 gene
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1 of 1 corroborated by 2+ sources
NAA15(2)
0.007 1.000 9.23e-3 1.04e-2 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 52 Nonsyndromic intellectual disability
1 gene
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1 of 1 corroborated by 2+ sources
ASH1L(4)
0.007 1.000 9.17e-3 1.03e-2 ✓ sig. —
Complex neurodevelopmental disorder Intellectual developmental disorder, autosomal dominant 5
1 gene
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1 of 1 corroborated by 2+ sources
SYNGAP1(2)
0.007 1.000 8.65e-3 9.79e-3 ✓ sig. —
Complex neurodevelopmental disorder Intellectual developmental disorder, autosomal dominant 53
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2A(2)
0.007 1.000 8.65e-3 9.79e-3 ✓ sig. —
Complex neurodevelopmental disorder Intellectual developmental disorder, autosomal dominant 51
1 gene
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1 of 1 corroborated by 2+ sources
KMT5B(2)
0.007 1.000 8.65e-3 9.79e-3 ✓ sig. —
Complex neurodevelopmental disorder Intellectual developmental disorder, autosomal dominant 57
1 gene
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1 of 1 corroborated by 2+ sources
TLK2(2)
0.007 1.000 8.65e-3 9.79e-3 ✓ sig. —
Cerebellar ataxia Intellectual developmental disorder, autosomal dominant 5
1 gene
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1 of 1 corroborated by 2+ sources
SYNGAP1(2)
0.008 1.000 7.81e-3 8.93e-3 ✓ sig. —
Cannabis abuse Intellectual developmental disorder, autosomal dominant 54
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2B(2)
0.009 1.000 7.49e-3 8.65e-3 ✓ sig. —
Congenital neurologic anomalies Intellectual developmental disorder, autosomal dominant 54
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2B(2)
0.009 1.000 7.43e-3 8.57e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities Tetralogy of fallot
1 gene
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1 of 1 corroborated by 2+ sources
NAA15(2)
0.009 1.000 7.23e-3 8.37e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 52 Lewy body disease
1 gene
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1 of 1 corroborated by 2+ sources
ASH1L(2)
0.010 1.000 6.13e-3 7.21e-3 ✓ sig. —
Hyperalgesia Intellectual developmental disorder, autosomal dominant 53
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2A(2)
0.011 1.000 5.75e-3 6.78e-3 ✓ sig. —
Brain aneurysm Intellectual developmental disorder, autosomal dominant 54
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2B(2)
0.011 1.000 5.68e-3 6.72e-3 ✓ sig. —
Hepatomegaly Intellectual developmental disorder, autosomal dominant 53
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2A(2)
0.017 1.000 3.74e-3 4.64e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities Syndromic intellectual disability
1 gene
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1 of 1 corroborated by 2+ sources
NAA15(2)
0.019 1.000 3.42e-3 4.29e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 51 Neural tube defect
1 gene
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1 of 1 corroborated by 2+ sources
KMT5B(2)
0.019 1.000 3.36e-3 4.22e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 58 Vulvar intraepithelial neoplasia
1 gene
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SET(1)
0.021 1.000 3.03e-3 3.86e-3 ✓ sig. —
Acute leukemia of ambiguous lineage Intellectual developmental disorder, autosomal dominant 58
1 gene
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SET(1)
0.023 1.000 2.71e-3 3.48e-3 ✓ sig. —
Hepatolenticular degeneration Intellectual developmental disorder, autosomal dominant 53
1 gene
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1 of 1 corroborated by 2+ sources
CAMK2A(3)
0.036 1.000 1.74e-3 2.42e-3 ✓ sig. —
Bladder exstrophy Intellectual developmental disorder, autosomal dominant 55, with seizures
1 gene
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1 of 1 corroborated by 2+ sources
NUS1(2)
0.045 1.000 1.36e-3 1.97e-3 ✓ sig. —

Showing 25 of 50 matching pairs, sorted by significance (descending). Click a column header to sort.