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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.
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Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▲ Shared cluster
Autistic behavior Delayed speech and language development
3 genes
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MED13(1), CTR9(1), POU3F3(1)
0.231 0.500 2.71e-9 2.26e-8 ✓ sig. —
Autistic behavior Generalized hypotonia
3 genes
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AP2M1(1), POU3F3(1), VAMP2(1)
0.200 0.375 7.59e-9 6.13e-8 ✓ sig. —
Autistic behavior Motor delay
2 genes
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MED13(1), CTR9(1)
0.182 0.667 9.00e-7 5.50e-6 ✓ sig. —
Autistic behavior Behavioral abnormality
2 genes
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PDZD8(1), CTR9(1)
0.091 0.222 2.72e-5 1.41e-4 ✓ sig. —
Autistic behavior Intellectual developmental disorder, autosomal dominant 61
1 gene
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MED13(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Hypertelorism
1 gene
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PDZD8(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay
1 gene
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ZNF462(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Disproportionate tall stature
1 gene
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PDZD8(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Intellectual developmental disorder dysmorphic
1 gene
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1 of 1 corroborated by 2+ sources
POU3F3(2)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Intellectual developmental disorder seizures epilepsy
1 gene
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1 of 1 corroborated by 2+ sources
AP2M1(3)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Intellectual developmental disorder, autosomal dominant 60, with seizures
1 gene
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AP2M1(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements
1 gene
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VAMP2(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Prominent metopic ridge
1 gene
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ZNF462(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Snijders blok-fisher syndrome
1 gene
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POU3F3(1)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —
Autistic behavior Weiss-kruszka syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ZNF462(6)
0.100 1.000 5.81e-4 1.00e-3 ✓ sig. —

Showing 15 of 15 matching pairs, sorted by significance (ascending). Click a column header to sort.