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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
Glycogen storage disease Ventricular dysfunction
3 genes
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3 of 3 corroborated by 2+ sources
TNNT2(2), PIK3CA(2), GAA(7)
0.037 0.081 1.81e-4 5.35e-4 ✓ sig. —
Dyslipidemias Osteopetrosis
2 genes
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2 of 2 corroborated by 2+ sources
TNFRSF11A(6), TCIRG1(8)
0.059 0.118 1.74e-4 5.23e-4 ✓ sig. —
Gastroparesis Internet addiction disorder
2 genes
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1 of 2 corroborated by 2+ sources
PRKG1(1), NRG1(2)
0.053 0.182 1.74e-4 5.23e-4 ✓ sig. —
Brain infarction Ventricular dysfunction
3 genes
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3 of 3 corroborated by 2+ sources
ALDH2(2), PLAT(2), SIRT1(2)
0.038 0.083 1.66e-4 5.01e-4 ✓ sig. —
Combined immunodeficiency disease Tubular aggregate myopathy
2 genes
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2 of 2 corroborated by 2+ sources
ORAI1(5), STIM1(5)
0.040 0.286 1.66e-4 5.00e-4 ✓ sig. —
Amblyopia Eye neoplasms
2 genes
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NPLOC4(1), OCA2(1)
0.056 0.167 1.65e-4 4.98e-4 ✓ sig. —
Esophageal disease Esotropia
2 genes
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2 of 2 corroborated by 2+ sources
SOD2(3), TRPV1(2)
0.051 0.200 1.64e-4 4.93e-4 ✓ sig. —
Cerebellar ataxia Diencephalic mesencephalic junction dysplasia
2 genes
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1 of 2 corroborated by 2+ sources
PCDH12(5), RNF14(1)
0.017 0.667 1.62e-4 4.89e-4 ✓ sig. —
B-cell chronic lymphocytic leukemia Diamond-blackfan anemia
2 genes
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2 of 2 corroborated by 2+ sources
TP53(2), RPS15(2)
0.045 0.250 1.56e-4 4.70e-4 ✓ sig. —
Lymphoid leukemia Ocular sarcoidosis
3 genes
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ALDH1A2(1), LIPC(1), HLA-DQB1(1)
0.036 0.107 1.55e-4 4.68e-4 ✓ sig. —
Hyperopia Vertebral, cardiac, renal, and limb defects syndrome
2 genes
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2 of 2 corroborated by 2+ sources
KYNU(6), NADSYN1(5)
0.024 0.500 1.55e-4 4.67e-4 ✓ sig. Cluster 386 →
Loeys-dietz syndrome Thoracic aortic aneurysm
2 genes
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2 of 2 corroborated by 2+ sources
FBN1(2), SMAD6(2)
0.061 0.125 1.53e-4 4.63e-4 ✓ sig. —
Gliosarcoma Hemangiosarcoma
2 genes
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1 of 2 corroborated by 2+ sources
TP53(2), VEGFA(1)
0.061 0.125 1.53e-4 4.63e-4 ✓ sig. —
Body weight Diabetic nephropathy type 2
2 genes
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2 of 2 corroborated by 2+ sources
CDKAL1(2), FTO(2)
0.061 0.125 1.53e-4 4.63e-4 ✓ sig. Cluster 73 →
Melas syndrome Mitochondrial encephalomyopathy
2 genes
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1 of 2 corroborated by 2+ sources
POLG(1), CYTB(2)
0.061 0.125 1.53e-4 4.63e-4 ✓ sig. —
Glycosylphosphatidylinositol biosynthesis defect Uranostaphyloschisis
2 genes
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1 of 2 corroborated by 2+ sources
MYO19(1), PIGW(2)
0.057 0.167 1.52e-4 4.59e-4 ✓ sig. —
Lipoma Uterine polyp
2 genes
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TERT(1), ACTRT3(1)
0.057 0.167 1.52e-4 4.59e-4 ✓ sig. —
Urinary system neoplasms Uterine polyp
2 genes
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TERT(1), ACTRT3(1)
0.057 0.167 1.52e-4 4.59e-4 ✓ sig. —
Hypospadias Porphyria cutanea tarda
2 genes
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GSTM1(1), CYP1A1(1)
0.042 0.286 1.51e-4 4.56e-4 ✓ sig. —
Cerebral arteriovenous malformations Costello syndrome
2 genes
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2 of 2 corroborated by 2+ sources
BRAF(3), KRAS(4)
0.059 0.154 1.51e-4 4.55e-4 ✓ sig. —
Congenital epicanthus Cryptorchidism
2 genes
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ANKRD11(1), KAT6B(1)
0.061 0.143 1.44e-4 4.36e-4 ✓ sig. —
Congenital hydrocephalus Fraser syndrome
2 genes
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1 of 2 corroborated by 2+ sources
WDR81(3), PTCH1(1)
0.061 0.143 1.44e-4 4.36e-4 ✓ sig. —
Paraquat lung disease Pulmonary fibrosis
2 genes
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2 of 2 corroborated by 2+ sources
SMAD7(2), SKIL(2)
0.018 0.667 1.43e-4 4.32e-4 ✓ sig. —
Epithelial ovarian carcinoma Keratosis
2 genes
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2 of 2 corroborated by 2+ sources
TP53(2), GSTM1(2)
0.054 0.200 1.42e-4 4.30e-4 ✓ sig. —
Hepatic insufficiency Pancreatic ductal carcinoma
2 genes
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NFE2L2(1), RELA(1)
0.051 0.222 1.40e-4 4.23e-4 ✓ sig. Cluster 153 →

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