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
Bouillaud’s disease Rosacea
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Rosacea Skeletal system disease
2 genes
Show details
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Rosacea Wheat allergic reaction
2 genes
Show details
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Achondrogenesis Spondylometaphyseal dysplasia
2 genes
Show details
2 of 2 corroborated by 2+ sources
TRIP11(2), COL2A1(6)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Avascular necrosis of femoral head Spondylometaphyseal dysplasia
2 genes
Show details
2 of 2 corroborated by 2+ sources
COL2A1(5), TRPV4(6)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Avascular necrosis of femoral head Osteonecrosis of medial femoral condyle
2 genes
Show details
2 of 2 corroborated by 2+ sources
COL2A1(5), TRPV4(5)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Cerebral sinovenous thrombosis Osteonecrosis of medial femoral condyle
2 genes
Show details
2 of 2 corroborated by 2+ sources
F2(2), F5(2)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Avascular necrosis of bone Avascular necrosis of femoral head
2 genes
Show details
2 of 2 corroborated by 2+ sources
COL2A1(5), TRPV4(5)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Avascular necrosis of bone Cerebral sinovenous thrombosis
2 genes
Show details
2 of 2 corroborated by 2+ sources
F2(2), F5(2)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Distal myopathy Multiminicore myopathy
2 genes
Show details
2 of 2 corroborated by 2+ sources
MYH7(3), TTN(3)
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. —
Bouillaud’s disease Cartilage disease
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Cartilage disease Skeletal system disease
2 genes
Show details
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Cartilage disease Wheat allergic reaction
2 genes
Show details
0.125 0.667 2.30e-6 1.26e-5 ✓ sig. Cluster 1 →
Atherosclerosis Dyslexia
8 genes
Show details
8 of 8 corroborated by 2+ sources
APOB(3), APOE(3), BCL3(2), HDAC9(3), HP(2), ABCG5(2), AHR(2), CETP(2)
0.036 0.072 2.28e-6 1.26e-5 ✓ sig. —
Endometrial hyperplasia Penile neoplasms
2 genes
Show details
2 of 2 corroborated by 2+ sources
TP53(2), KRAS(2)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Cecal neoplasms Endometrial hyperplasia
2 genes
Show details
2 of 2 corroborated by 2+ sources
CTNNB1(2), KRAS(2)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Myelomonocytic leukemia Neurofibromatosis-noonan syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
NF1(6), PTPN11(4)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Cleft lip and cleft of alveolar process of maxilla Congenital skin anomaly
2 genes
Show details
TP63(1), IRF6(1)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Craniodiaphyseal dysplasia Mainzer-saldino disease
2 genes
Show details
2 of 2 corroborated by 2+ sources
IFT140(2), WDR19(6)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Goldenhar syndrome Hemifacial microsomia
2 genes
Show details
1 of 2 corroborated by 2+ sources
FOXI3(1), SF3B2(2)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. Cluster 48 →
Congenital malformation syndromes predominantly affecting facial appearance Martsolf syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. Cluster 48 →
Martsolf syndrome Warburg micro syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. Cluster 48 →
Cleft lip and cleft of alveolar process of maxilla Skin abnormalities
2 genes
Show details
2 of 2 corroborated by 2+ sources
TP63(2), IRF6(2)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —
Intestinal pseudo-obstruction Tricuspid valve disease
2 genes
Show details
MYH11(1), NDE1(1)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. Cluster 220 →
Kidney and ureter calculus Ureterolithiasis
2 genes
Show details
2 of 2 corroborated by 2+ sources
RGS14(2), CYP24A1(2)
0.154 0.500 2.28e-6 1.26e-5 ✓ sig. —

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