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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
dilated cardiomyopathy 1J Sensorineural deafness with dilated cardiomyopathy
1 gene
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1 of 1 corroborated by 2+ sources
EYA4(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
dilated cardiomyopathy 1KK MYPN-related myopathy
1 gene
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MYPN(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
dilated cardiomyopathy 1O Intellectual disability and myopathy syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ABCC9(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 234 →
dilated cardiomyopathy 1O hypertrichotic osteochondrodysplasia Cantu type
1 gene
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ABCC9(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 234 →
dilated cardiomyopathy 1S Myosin storage myopathy
1 gene
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1 of 1 corroborated by 2+ sources
MYH7(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 89 →
dilated cardiomyopathy 1S MYH7-related skeletal myopathy
1 gene
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MYH7(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 89 →
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Severe lipodystrophic laminopathy
1 gene
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1 of 1 corroborated by 2+ sources
LMNA(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 65 →
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Lipoatrophic diabetes mellitus
1 gene
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1 of 1 corroborated by 2+ sources
LMNA(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 65 →
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Malouf syndrome
1 gene
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1 of 1 corroborated by 2+ sources
LMNA(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 65 →
Direct inguinal hernia loeys-dietz syndrome 2
1 gene
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1 of 1 corroborated by 2+ sources
TGFBR2(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Distal anoctaminopathy gnathodiaphyseal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
ANO5(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 290 →
Distal axonal motor neuropathy-myofibrillar myopathy syndrome neuronopathy, distal hereditary motor, autosomal dominant
1 gene
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1 of 1 corroborated by 2+ sources
HSPB8(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Distal nebulin myopathy Nebulin-related myopathy
1 gene
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1 of 1 corroborated by 2+ sources
NEB(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 51 →
Distal nebulin myopathy nemaline myopathy 2
1 gene
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1 of 1 corroborated by 2+ sources
NEB(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 51 →
Ditra syndrome Von zumbuzschs disease
1 gene
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1 of 1 corroborated by 2+ sources
IL36RN(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Dkc1-related disorder dyskeratosis congenita, x-linked
1 gene
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1 of 1 corroborated by 2+ sources
DKC1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 64 →
Dominant beta-thalassemia Hemoglobin c disease
1 gene
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1 of 1 corroborated by 2+ sources
HBB(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 19 →
Dominant beta-thalassemia Hemoglobin c beta thalassemia
1 gene
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1 of 1 corroborated by 2+ sources
HBB(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 19 →
Dominant beta-thalassemia Hemoglobin d disease
1 gene
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1 of 1 corroborated by 2+ sources
HBB(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 19 →
Dominant beta-thalassemia Hemoglobin e beta thalassemia
1 gene
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1 of 1 corroborated by 2+ sources
HBB(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 19 →
Dominant dystrophic epidermolysis bullosa with absence of skin Dominant dystrophic epidermolysis bullosa, albopapular type
1 gene
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1 of 1 corroborated by 2+ sources
COL7A1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 160 →
Dominant hereditary optic atrophy OPA1-related optic atrophy with or without extraocular features
1 gene
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1 of 1 corroborated by 2+ sources
OPA1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Donohue syndrome Insulin-resistant diabetes mellitus with acanthosis nigricans
1 gene
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1 of 1 corroborated by 2+ sources
INSR(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Donohue syndrome Type a insulin resistance syndrome
1 gene
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1 of 1 corroborated by 2+ sources
INSR(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Dopamine transporter deficiency syndrome SLC6A3-related dopamine transporter deficiency syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SLC6A3(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 392 →

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