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
amyotrophic lateral sclerosis, susceptibility to, 25 Genetic neurodegenerative disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIF5A(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Analbuminemia Anuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 372 →
Analbuminemia Hyperthyroxinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Anastomosing haemangioma Cerebrofacial arteriovenous metameric syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNA14(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 40 →
Angiofollicular ganglionic hyperplasia Intracranial arteriovenous malformation
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 126 →
Angiolymphoid hyperplasia Intracranial arteriovenous malformation
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 126 →
Ankylosis Antley-bixler syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 85 →
Antithrombin deficiency Craniocerebral trauma
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 197 →
Antithrombin deficiency Hereditary antithrombin deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 197 →
Antley-bixler syndrome P450 oxidoreductase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
POR(8)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 85 →
Antley-bixler syndrome Beare-stevenson cutis gyrata syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 85 →
Antley-bixler syndrome Cutis gyrata syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 85 →
Anuria quebec platelet disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLAU(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Anuria Blood protein disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 372 →
Anuria Congenital analbuminemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 372 →
Anuria Dysalbuminemic hyperthyroxinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 372 →
Aplasia and myelodysplasia Congenital bone marrow failure syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SRP72(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 3 →
Aplasia of lacrimal and salivary glands Lacrimoauriculodentodigital syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF10(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Aplasia of lacrimal and salivary glands Ladd syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF10(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Apnea Butyrylcholinesterase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCHE(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 378 →
Apnea Trismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCHE(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 378 →
Apolipoprotein a-i amyloidosis Ataxia with vitamin e deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOA1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Apolipoprotein c-iii deficiency Cholesterol ester transfer protein deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOC3(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Apolipoprotein c-iii deficiency Hyperalphalipoproteinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOC3(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Arachnoid cysts sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
1 gene
Show details
1 of 1 corroborated by 2+ sources
GPHN(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —

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