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
Erectile dysfunction Heart disease
6 genes
Show details
3 of 6 corroborated by 2+ sources
CDH13(1), VEGFA(2), NOS3(3), EDNRA(3), TDRD15(1), ZC3HC1(1)
0.030 0.098 2.37e-5 1.11e-4 ✓ sig. —
Aortic arch syndrome Retinopathy of prematurity
2 genes
Show details
HLA-DRB1(1), HLA-B(1)
0.080 0.333 2.40e-5 1.13e-4 ✓ sig. —
Acromesomelic dysplasia Chondrodysplasia
2 genes
Show details
2 of 2 corroborated by 2+ sources
BMPR1B(3), GDF5(5)
0.087 0.286 2.40e-5 1.13e-4 ✓ sig. —
Asbestosis Osteolysis
2 genes
Show details
2 of 2 corroborated by 2+ sources
SPP1(2), TNF(2)
0.087 0.286 2.40e-5 1.13e-4 ✓ sig. —
Atrioventricular block Hereditary bundle branch system defect
2 genes
Show details
1 of 2 corroborated by 2+ sources
TRPM4(2), NKX2-5(1)
0.087 0.286 2.40e-5 1.13e-4 ✓ sig. Cluster 4 →
Atrioventricular block Emery-dreifuss muscular dystrophy
2 genes
Show details
2 of 2 corroborated by 2+ sources
LMNA(6), SYNE1(6)
0.087 0.286 2.40e-5 1.13e-4 ✓ sig. —
Hodgkin disease Hyper-igm immunodeficiency syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
CD40LG(5), CD40(6)
0.087 0.286 2.40e-5 1.13e-4 ✓ sig. Cluster 131 →
Amphetamine or sympathomimetic abuse Non-organic psychosis
5 genes
Show details
5 of 5 corroborated by 2+ sources
GSTP1(2), NPY1R(2), OPRM1(2), PICK1(2), SLC6A9(2)
0.035 0.072 2.40e-5 1.13e-4 ✓ sig. —
Developmental delay with variable intellectual disability Intellectual disability
2 genes
Show details
2 of 2 corroborated by 2+ sources
TCF20(5), JARID2(5)
0.026 1.000 2.40e-5 1.13e-4 ✓ sig. —
Keratinocyte carcinoma Primary adrenal insufficiency
2 genes
Show details
CUX1(1), MYL10(1)
0.026 1.000 2.47e-5 1.16e-4 ✓ sig. —
Anhedonia Panic disorder
3 genes
Show details
COMT(1), HTR1A(1), CRH(1)
0.052 0.115 2.47e-5 1.16e-4 ✓ sig. Cluster 156 →
Gouty arthritis Mucositis
2 genes
Show details
2 of 2 corroborated by 2+ sources
IL1B(2), IL1RN(2)
0.091 0.250 2.47e-5 1.16e-4 ✓ sig. —
Uterine prolapse Visual impairment
2 genes
Show details
EFEMP1(1), PNPT1(1)
0.091 0.250 2.47e-5 1.16e-4 ✓ sig. Cluster 146 →
Congenital aneurysm of ascending aorta Tricuspid valve disease
2 genes
Show details
MYH11(1), NDE1(1)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Intervertebral disc disease Trigeminal neuralgia
2 genes
Show details
2 of 2 corroborated by 2+ sources
IL1B(2), TNF(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. Cluster 180 →
Esotropia Papilloma
2 genes
Show details
2 of 2 corroborated by 2+ sources
SOD2(2), PTGS2(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
monogenic diabetes Paralysis
2 genes
Show details
2 of 2 corroborated by 2+ sources
INS(2), SIRT1(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Hydronephrosis Hypertensive heart disease
2 genes
Show details
PDILT(1), UMOD(1)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Hyperoxaluria Pleural diseases
2 genes
Show details
2 of 2 corroborated by 2+ sources
IL6(2), CCL2(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Childhood absence epilepsy Lennox-gastaut syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
GABRG2(2), GABRB3(4)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. Cluster 47 →
Childhood absence epilepsy Idiopathic generalized epilepsy
2 genes
Show details
2 of 2 corroborated by 2+ sources
GABRA1(3), SLC2A1(4)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. Cluster 47 →
Majewski syndrome Saldino-noonan syndrome
2 genes
Show details
NEK1(1), DYNC2H1(1)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. Cluster 22 →
Nanophthalmos Septo-optic dysplasia
2 genes
Show details
2 of 2 corroborated by 2+ sources
SOX2(3), OTX2(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Endometrial hyperplasia Intestinal neoplasms
2 genes
Show details
2 of 2 corroborated by 2+ sources
CTNNB1(2), APC(2)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. —
Angina pectoris Esotropia
2 genes
Show details
1 of 2 corroborated by 2+ sources
TNF(2), CXCL8(1)
0.095 0.200 2.50e-5 1.17e-4 ✓ sig. Cluster 76 →

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