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
Dkc1-related disorder Hoyeraal hreidarsson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DKC1(5)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 64 →
Double outlet right ventricle Interrupted aortic arch
1 gene
Show details
NKX2-5(1)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Double outlet right ventricle NKX2.5-related congenital, conduction and myopathic heart disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
NKX2-5(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
duane retraction syndrome 2 Robinow syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHN1(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 127 →
dyskeratosis congenita and related telomere biology disorder Telomere-related pulmonary fibrosis and/or bone marrow failure
1 gene
Show details
1 of 1 corroborated by 2+ sources
RPA1(5)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 64 →
dyskeratosis congenita, autosomal dominant 3 Hoyeraal hreidarsson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TINF2(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
dyskeratosis congenita, x-linked Hoyeraal hreidarsson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DKC1(5)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 64 →
dysosteosclerosis Osteosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCIRG1(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome Osteosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBCE(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 108 →
EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition Secondary polycythemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
EGLN1(4)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Eiken skeletal dysplasia Metaphyseal chondrodysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTH1R(6)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
encephalopathy, progressive, with amyotrophy and optic atrophy Osteosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBCE(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 108 →
Capillary malformation-arteriovenous malformation EPHB4-associated vascular malformation spectrum
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPHB4(6)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Argininosuccinic aciduria Urea cycle disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ASL(7)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 367 →
Arhinia-choanal atresia-microphthalmia syndrome Facial nerve disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMCHD1(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 313 →
Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome Rhabdomyolysis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANO5(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 290 →
Ataxia, spastic, autosomal recessive with optic atrophy and impaired intellect Charcot-marie-tooth disease, x-linked
1 gene
Show details
SACS(1)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
ATF6-related retinopathy Congenital nystagmus
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATF6(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
ATM-related cancer predisposition B-cell chronic lymphocytic leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATM(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
atypical hemolytic-uremic syndrome with B factor anomaly C3 glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CFB(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 359 →
atypical hemolytic-uremic syndrome with B factor anomaly Mesangiocapillary glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CFB(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. Cluster 359 →
atypical hemolytic-uremic syndrome with C3 anomaly C3 glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
C3(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
atypical hemolytic-uremic syndrome with C3 anomaly Mesangiocapillary glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
C3(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
atypical hemolytic-uremic syndrome with DGKE deficiency Mesangiocapillary glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
DGKE(2)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —
Auricle malformation Branchial arch abnormalities syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KMT2D(3)
0.111 1.000 5.20e-4 1.06e-3 ✓ sig. —

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