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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
Developmental and epileptic encephalopathy Seizures
33 genes
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29 of 33 corroborated by 2+ sources
FOXG1(3), ATP1A3(5), ABAT(4), HCN1(5), KCNQ2(7), RBFOX1(2), SCN8A(7), SLC6A1(2), GABRG2(6), CHRNA4(2), GABRA1(5), GRIA3(1) +21 more
0.100 0.234 4.89e-31 1.54e-29 ✓ sig. —
Biliary cholangitis Sclerosing cholangitis
34 genes
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12 of 34 corroborated by 2+ sources
SH2B3(1), ETS1(1), HLA-DQA1(2), HLA-DRA(1), IKZF1(1), ATXN2(1), HLA-DQB1(1), ATG5(1), CCR6(1), CCL20(1), CD226(1), CEP43(1) +22 more
0.099 0.231 4.27e-31 1.34e-29 ✓ sig. —
Cone-rod dystrophy Stargardt disease
16 genes
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6 of 16 corroborated by 2+ sources
ABCA4(7), CNGB3(2), PRPH2(4), CRB1(1), CRX(8), PROM1(6), RPE65(1), GPHN(1), EYS(1), OPA1(1), KCNV2(1), CERKL(1) +4 more
0.184 0.571 4.14e-31 1.30e-29 ✓ sig. Cluster 7 →
Ciliary dyskinesia, with or without situs inversus Polynesian bronchiectasis
9 genes
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MBL2(1), DNAH5(1), CCDC40(1), DNAH11(1), DNAI1(1), DNAAF3(1), DNAAF19(1), DNAAF4(1), DRC1(1)
0.750 1.000 4.11e-31 1.30e-29 ✓ sig. Cluster 9 →
Cataract Congenital total cataract
16 genes
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16 of 16 corroborated by 2+ sources
LSS(6), CRYBB2(6), PGRMC1(2), CRYAA(6), EPHA2(6), GJA8(5), DNMBP(6), HSF4(5), LIM2(6), MIP(6), GCNT2(6), FYCO1(5) +4 more
0.079 1.000 3.88e-31 1.23e-29 ✓ sig. Cluster 43 →
Duodenal ulcer Gastric ulcer
16 genes
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4 of 16 corroborated by 2+ sources
CCKBR(1), FUT2(1), MECOM(1), PRKAA1(1), TTC33(1), PTGS2(2), ABO(3), NOS2(2), JRK(1), PSCA(3), PLCL2(1), ZNF800(1) +4 more
0.213 0.432 3.85e-31 1.22e-29 ✓ sig. —
Graves disease Thyroid disease
20 genes
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10 of 20 corroborated by 2+ sources
FAM76B(1), HLA-DQA1(2), ICOS(1), VEGFA(2), HLA-DQB1(2), CCR6(1), BACH2(1), CEP43(1), CTLA4(3), IL2RA(1), PTPN22(3), TG(3) +8 more
0.150 0.377 3.24e-31 1.03e-29 ✓ sig. Cluster 39 →
Congenital stationary night blindness Oguchi disease
10 genes
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10 of 10 corroborated by 2+ sources
CACNA1F(2), PDE6B(4), TRPM1(3), RHO(4), GNB3(3), GNAT1(3), GRM6(3), LRIT3(3), NYX(3), SLC24A1(3)
0.588 0.833 3.21e-31 1.02e-29 ✓ sig. Cluster 151 →
Atherosclerosis Ischemic heart disease
29 genes
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24 of 29 corroborated by 2+ sources
APOA1(2), ABCA1(2), APOB(2), APOE(3), LDLR(3), SERPINE1(2), VEGFA(2), NOS3(2), AGER(2), ESR1(2), MTHFR(1), PON1(2) +17 more
0.111 0.244 2.73e-31 8.67e-30 ✓ sig. —
Skin cancer Vitiligo
24 genes
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9 of 24 corroborated by 2+ sources
FADS1(1), FADS2(1), FAM76B(1), FOXP1(3), HERC2(1), HLA-DQA1(2), HLA-DRB1(2), ICOS(1), RALY(1), IRF4(1), CCR6(3), BACH2(3) +12 more
0.129 0.289 2.50e-31 7.96e-30 ✓ sig. —
Hyperlipoproteinemia Ischemic heart disease
21 genes
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12 of 21 corroborated by 2+ sources
AMPD1(1), ABCA1(2), ABCG8(1), APOB(2), APOE(5), EPHX2(1), LDLR(2), LIPC(2), NOS3(1), ADRB3(1), HMGCR(2), IRS1(1) +9 more
0.111 0.525 2.46e-31 7.84e-30 ✓ sig. —
Brain ischemia Pulmonary fibrosis
22 genes
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22 of 22 corroborated by 2+ sources
CAT(2), ACE(2), PLAU(2), HSPA1B(2), IGF1(2), IL1A(2), IL1B(2), PARP1(2), STAT3(2), TNF(2), IL6(2), PTGS2(2) +10 more
0.141 0.314 2.21e-31 7.05e-30 ✓ sig. —
Hashimoto disease Thyroid disease
15 genes
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2 of 15 corroborated by 2+ sources
SH2B3(1), FAM76B(1), HLA-DQA1(1), ICOS(1), ATXN2(1), BACH2(1), CTLA4(3), IL2RA(1), PTPN22(1), TG(3), STAT4(1), CD69(1) +3 more
0.227 0.556 2.15e-31 6.86e-30 ✓ sig. Cluster 39 →
Ventricular fibrillation Wolff-parkinson-white syndrome
16 genes
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2 of 16 corroborated by 2+ sources
ACTN2(1), JUP(1), RBM20(1), TRPM4(1), DSP(1), DPP6(3), KCNJ2(1), CACNA1C(1), MYH6(1), KCNH2(1), RYR2(1), SCN5A(3) +4 more
0.222 0.444 1.06e-31 3.40e-30 ✓ sig. Cluster 4 →
Distal hereditary motor neuropathy Spinal muscular atrophy
15 genes
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15 of 15 corroborated by 2+ sources
TRPV4(4), VRK1(3), SIGMAR1(4), BICD2(4), DYNC1H1(5), ATP7A(3), HSPB1(6), REEP1(7), PLEKHG5(4), GARS1(6), HSPB8(6), IGHMBP2(4) +3 more
0.254 0.417 1.03e-31 3.30e-30 ✓ sig. Cluster 15 →
Neuropathy, ataxia, and retinitis pigmentosa Postaxial polydactyly
11 genes
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1 of 11 corroborated by 2+ sources
ND1(1), ND2(1), ATP6(2), COX3(1), ATP8(1), COX1(1), ND5(1), COX2(1), ND3(1), ND4(1), ND4L(1)
0.458 0.846 9.54e-32 3.06e-30 ✓ sig. Cluster 32 →
Cardiofaciocutaneous syndrome Costello syndrome
10 genes
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10 of 10 corroborated by 2+ sources
BRAF(7), KRAS(8), NRAS(3), SHOC2(2), RAF1(2), PTPN11(3), SOS1(2), MAP2K1(7), HRAS(6), MAP2K2(8)
0.625 0.833 9.17e-32 2.95e-30 ✓ sig. Cluster 42 →
Keratinocyte carcinoma Skin disease
26 genes
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TERT(1), BNC2(1), CUX1(1), HERC2(1), HLA-DQA1(1), HLA-DRB1(1), MYL10(1), SPMIP7(1), TRPS1(1), RALY(1), IRF4(1), KRT5(1) +14 more
0.114 0.338 7.92e-32 2.55e-30 ✓ sig. Cluster 29 →
Hereditary parkinson disease Parkinson disease
24 genes
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22 of 24 corroborated by 2+ sources
HLA-DRA(3), LRRK2(7), MAPT(5), PRKN(8), GSTP1(2), ND1(1), SNCA(8), ATXN2(3), ATXN3(3), PARK7(8), GIGYF2(5), NR4A2(4) +12 more
0.045 0.857 7.89e-32 2.55e-30 ✓ sig. —
Gilbert syndrome Lucey-driscoll syndrome
9 genes
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1 of 9 corroborated by 2+ sources
UGT1A10(1), UGT1A8(1), UGT1A9(1), UGT1A1(4), UGT1A6(1), UGT1A3(1), UGT1A4(1), UGT1A5(1), UGT1A7(1)
0.818 1.000 7.47e-32 2.42e-30 ✓ sig. Cluster 260 →
Lucey-driscoll syndrome Perinatal disease
9 genes
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9 of 9 corroborated by 2+ sources
UGT1A10(2), UGT1A8(2), UGT1A9(2), UGT1A1(3), UGT1A6(2), UGT1A3(2), UGT1A4(2), UGT1A5(2), UGT1A7(2)
0.818 1.000 7.47e-32 2.42e-30 ✓ sig. Cluster 260 →
Crigler-najjar syndrome Gilbert syndrome
9 genes
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1 of 9 corroborated by 2+ sources
UGT1A10(1), UGT1A8(1), UGT1A9(1), UGT1A1(6), UGT1A6(1), UGT1A3(1), UGT1A4(1), UGT1A5(1), UGT1A7(1)
0.818 1.000 7.47e-32 2.42e-30 ✓ sig. Cluster 260 →
Crigler-najjar syndrome Perinatal disease
9 genes
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9 of 9 corroborated by 2+ sources
UGT1A10(2), UGT1A8(2), UGT1A9(2), UGT1A1(7), UGT1A6(2), UGT1A3(2), UGT1A4(2), UGT1A5(2), UGT1A7(2)
0.818 1.000 7.47e-32 2.42e-30 ✓ sig. Cluster 260 →
Costello syndrome Noonan syndrome
12 genes
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10 of 12 corroborated by 2+ sources
BRAF(7), KRAS(8), NRAS(7), SHOC2(7), RAF1(7), PTPN11(7), SOS1(7), MAP2K1(6), HRAS(6), MAP2K2(4), SPRED1(1), LRRC56(1)
0.308 0.923 6.51e-32 2.12e-30 ✓ sig. Cluster 42 →
Macular and posterior pole degeneration Macular degeneration
13 genes
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6 of 13 corroborated by 2+ sources
CFI(3), HERC2(1), C3(3), CD46(1), PDGFB(1), RPL3(1), CETP(1), CFH(3), RDH5(1), ARMS2(3), C9(3), SKIC2(1) +1 more
0.191 1.000 5.80e-32 1.89e-30 ✓ sig. Cluster 187 →

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