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
Congenital muscular dystrophy due to dystroglycanopathy muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
combined immunodeficiency due to STIM1 deficiency Tubular aggregate myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
STIM1(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 217 →
complex movement disorder with or without neurodevelopmental features Torsion dystonia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HPCA(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 167 →
Congenital atransferrinemia Hereditary hemochromatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TF(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital atransferrinemia Iron overload
1 gene
Show details
1 of 1 corroborated by 2+ sources
TF(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital cardiovascular anomaly immunodeficiency 11b with atopic dermatitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CARD11(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 327 →
Congenital cardiovascular anomaly severe combined immunodeficiency due to CARD11 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CARD11(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 327 →
Congenital cardiovascular anomaly Fanconi anemia complementation group C
1 gene
Show details
1 of 1 corroborated by 2+ sources
FANCC(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 327 →
Congenital cleft hand Klippel-trenaunay syndrome
1 gene
Show details
DLX5(1)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital factor xii deficiency Hereditary angioedema
1 gene
Show details
1 of 1 corroborated by 2+ sources
F12(6)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital glaucoma CYP1B1-related glaucoma with or without anterior segment dysgenesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP1B1(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Bockenheimer syndrome Congenital glaucoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
TEK(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital glaucoma Mucocutaneous venous malformations
1 gene
Show details
1 of 1 corroborated by 2+ sources
TEK(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital glucokinase-related hyperinsulinism Prediabetes
1 gene
Show details
1 of 1 corroborated by 2+ sources
GCK(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Congenital high-molecular-weight kininogen deficiency Extravasation of diagnostic and therapeutic materials
1 gene
Show details
1 of 1 corroborated by 2+ sources
KNG1(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 250 →
Congenital high-molecular-weight kininogen deficiency Hereditary angioedema
1 gene
Show details
1 of 1 corroborated by 2+ sources
KNG1(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 250 →
Binge eating disorder hypercholesterolemia, autosomal dominant, type B
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOB(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 140 →
Bone marrow neoplasms Hepatic veno occlusive disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSF3(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Bone marrow neoplasms Leiomyosarcoma
1 gene
Show details
CSF3(1)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Bonnevie-ullrich syndrome Esophageal stenosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOD2(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Benign hereditary chorea Brain-lung-thyroid syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NKX2-1(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Brainstem atrophy Mucolipidosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MCOLN1(7)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 91 →
Branched-chain keto acid dehydrogenase kinase deficiency Maple syrup urine disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCKDK(5)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Asymmetric crying face association Branchiootorenal syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EYA1(5)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 145 →
Acro-dermo-ungual-lacrimal-tooth syndrome Breast disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 27 →

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