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
Blood protein disorder 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. —
Blue cone monochromatism Tritanopia
1 gene
Show details
1 of 1 corroborated by 2+ sources
OPN1SW(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 214 →
Blue cone monochromatism red color blindness
1 gene
Show details
1 of 1 corroborated by 2+ sources
OPN1LW(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 214 →
Blue cone monochromatism red-green color blindness
1 gene
Show details
1 of 1 corroborated by 2+ sources
OPN1MW(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 214 →
Bnar syndrome Trigonocephaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
FREM1(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 185 →
Body skin hyperlaxity Combined deficiency of vitamin k-dependent clotting factors
1 gene
Show details
1 of 1 corroborated by 2+ sources
GGCX(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Bohring-opitz-like syndrome Cold-induced sweating syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KLHL7(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 331 →
Bohring-opitz-like syndrome Crisponi syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KLHL7(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 331 →
Bone osteosarcoma CHEK2-related cancer predisposition
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHEK2(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 3 →
Adrenocortical carcinoma Bone osteosarcoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP53(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 3 →
Bone osteosarcoma Choroid plexus carcinoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP53(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 3 →
Bor syndrome Cayler cardiofacial syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EYA1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 145 →
Brachydactyly-syndactyly syndrome Synpolydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
HOXD13(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 397 →
Brachymesophalangy Synpolydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
HOXD13(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 397 →
Brachyolmia Congenital benign spinal muscular atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPV4(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 215 →
Brachyolmia Brachyrachia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPV4(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 215 →
Brachyolmia Digital arthropathy-brachydactyly, familial
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPV4(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 215 →
Brachyolmia Parastremmatic dwarfism
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPV4(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 215 →
Brachyolmia Scapuloperoneal spinal muscular atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRPV4(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 215 →
Brain anomalies ectodermal dysplasia skeletal malformations hirschsprung disease syndrome Congenital palmoplantar and perioral keratoderma of olmsted
1 gene
Show details
MBTPS2(1)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 332 →
Brain malformations Chromosome 1p32-p31 deletion syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFIA(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Brain malformations Zhu-tokita-takenouchi-kim syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SON(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Brain tumor-polyposis syndrome Desmoid tumor
1 gene
Show details
1 of 1 corroborated by 2+ sources
APC(6)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 41 →
Brain tumor-polyposis syndrome Turcot syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
APC(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Branchial arch abnormalities syndrome Vissers-bodmer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KMT2D(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 144 →

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