Log in to save this analysis

Save This Analysis

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
Anterior segment mesenchymal dysgenesis Congenital cataract microcornea with corneal opacity
1 gene
Show details
1 of 1 corroborated by 2+ sources
PXDN(3)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Congenital leukocyte adherence deficiency Coronary restenosis
1 gene
Show details
ITGB2(1)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Bicuspid aortic valve Congenital radioulnar synostosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMAD6(4)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Corpus callosum agenesis Partington syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PAK3(2)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Intestinal disease Spectrum and myeloid neoplasm risk
1 gene
Show details
1 of 1 corroborated by 2+ sources
SAMD9(3)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Metabolic bone disorder Syndactyly of the toes
1 gene
Show details
DHCR7(1)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Hyperemia Partial adenosine deaminase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADA(2)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Nephrosclerosis Periapical periodontitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF2(2)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Perrault syndrome Progressive arterial occlusive disease with hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
DAP3(3)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. Cluster 336 →
Fanconi-bickel syndrome Permanent neonatal diabetes mellitus
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC2A2(5)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. Cluster 36 →
Growth hormone insensitivity syndrome with immune dysregulation Pancytopenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERCC6L2(4)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
Anaplasia Cholangitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
HIF1A(2)
0.063 0.500 1.82e-3 2.68e-3 ✓ sig. —
acute myeloid leukemia Mastocytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CEBPA(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
Alveolar capillary dysplasia Mastocytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
FOXF1(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
amyotrophic lateral sclerosis type 19 Internet addiction disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERBB4(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
Anterior cruciate ligament injury Scleroderma
1 gene
Show details
CNR2(1)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
Apolipoprotein a5 deficiency Hypertriglyceridemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOA5(5)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. Cluster 254 →
Aromatic l-amino-acid decarboxylase deficiency Exostoses
1 gene
Show details
1 of 1 corroborated by 2+ sources
DDC(4)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development Epithelial ovarian carcinoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
PPP3CA(4)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
atypical hemolytic-uremic syndrome with B factor anomaly Sickle cell anemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CFB(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
autoimmune lymphoproliferative syndrome type 1 Diabetic angiopathies
1 gene
Show details
1 of 1 corroborated by 2+ sources
FASLG(3)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. Cluster 368 →
autoimmune lymphoproliferative syndrome type 1 Diabetic peripheral angiopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
FASLG(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. Cluster 368 →
Guanidinoacetate methyltransferase deficiency Hereditary parkinson disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
GAMT(3)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
Hepatic lipase deficiency Lymphoid leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
LIPC(4)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —
hereditary spherocytosis Internet addiction disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANK1(2)
0.034 1.000 1.82e-3 2.68e-3 ✓ sig. —

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