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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
Charcot-marie-tooth disease Giant axonal neuropathy
2 genes
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2 of 2 corroborated by 2+ sources
GAN(7), DCAF8(6)
0.015 1.000 7.29e-5 2.61e-4 ✓ sig. —
Ocular anomalies with axonal neuropathy and developmental delay Parenti-mignot neurodevelopmental syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CHD5(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
1p36.33 duplication syndrome Ocular anomalies with axonal neuropathy and developmental delay
1 gene
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1 of 1 corroborated by 2+ sources
ATAD3A(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Anterior segment dysgenesis Axonal neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
GBF1(2)
0.042 1.000 1.49e-3 2.31e-3 ✓ sig. —
Axonal neuropathy Partial epilepsy
1 gene
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GBF1(1)
0.022 1.000 2.86e-3 3.81e-3 ✓ sig. —
Arthritis Giant axonal neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
GAN(7)
0.036 0.500 3.37e-3 4.37e-3 ✓ sig. —
Axonal neuropathy Congenital cataract
1 gene
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1 of 1 corroborated by 2+ sources
GBF1(2)
0.016 1.000 3.90e-3 4.94e-3 ✓ sig. —
Ocular anomalies with axonal neuropathy and developmental delay Pontocerebellar hypoplasia
1 gene
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1 of 1 corroborated by 2+ sources
ATAD3A(5)
0.030 0.500 4.02e-3 5.09e-3 ✓ sig. —
Axonal neuropathy Generalized epilepsy
1 gene
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GBF1(1)
0.015 1.000 4.22e-3 5.32e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Ocular anomalies with axonal neuropathy and developmental delay
1 gene
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1 of 1 corroborated by 2+ sources
ATAD3A(2)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Axonal neuropathy Digestive system disease
1 gene
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GBF1(1)
0.011 1.000 6.04e-3 7.27e-3 ✓ sig. —
Giant axonal neuropathy Peripheral nervous system disease
1 gene
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1 of 1 corroborated by 2+ sources
GAN(7)
0.018 0.500 6.87e-3 8.15e-3 ✓ sig. Cluster 243 →
Giant axonal neuropathy Non-neoplastic peripheral nervous system disease
1 gene
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1 of 1 corroborated by 2+ sources
GAN(7)
0.018 0.500 7.00e-3 8.29e-3 ✓ sig. Cluster 243 →
Axonal neuropathy with neuromyotonia Myopathy
1 gene
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1 of 1 corroborated by 2+ sources
HINT1(3)
0.009 1.000 7.27e-3 8.58e-3 ✓ sig. Cluster 14 →
Axonal neuropathy with neuromyotonia Charcot-marie-tooth disease
1 gene
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1 of 1 corroborated by 2+ sources
HINT1(5)
0.008 1.000 8.57e-3 9.90e-3 ✓ sig. —
Axonal neuropathy with neuromyotonia Peripheral neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
HINT1(3)
0.005 1.000 1.25e-2 1.39e-2 ✓ sig. —
Axonal neuropathy with neuromyotonia Respiratory system disease
1 gene
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1 of 1 corroborated by 2+ sources
HINT1(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Neuroblastoma Ocular anomalies with axonal neuropathy and developmental delay
1 gene
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1 of 1 corroborated by 2+ sources
CHD5(2)
0.007 0.500 1.95e-2 2.13e-2 ✓ sig. —
Axonal neuropathy with neuromyotonia Venous thromboembolism
1 gene
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1 of 1 corroborated by 2+ sources
HINT1(4)
0.003 1.000 2.22e-2 2.40e-2 ✓ sig. —
Giant axonal neuropathy Peripheral neuropathy
1 gene
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1 of 1 corroborated by 2+ sources
GAN(7)
0.005 0.500 2.48e-2 2.65e-2 ✓ sig. Cluster 243 →

Showing 20 of 20 matching pairs, sorted by significance (ascending). Click a column header to sort.