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
Hereditary steroid-resistant nephrotic syndrome idiopathic multidrug-resistant nephrotic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DAAM2(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
immunodeficiency-centromeric instability-facial anomalies syndrome 3 Triple negative breast cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDCA7(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
Genetic steroid-resistant nephrotic syndrome inherited focal segmental glomerulosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CD2AP(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
Hereditary steroid-resistant nephrotic syndrome inherited focal segmental glomerulosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CD2AP(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
Intellectual developmental disorder microcephaly strabismus behaviora Strabismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
POGZ(3)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
intellectual disability, autosomal dominant 42 Strabismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNB1(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
krabbe disease Strabismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
GALC(2)
0.029 1.000 2.21e-3 3.11e-3 ✓ sig. —
Congenital disorder of glycosylation Myasthenic syndrome
3 genes
Show details
3 of 3 corroborated by 2+ sources
ALG2(4), ALG14(4), DPAGT1(6)
0.022 0.075 2.14e-3 3.04e-3 ✓ sig. —
Concentric hypertrophic cardiomyopathy Short qt syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CACNA1C(3)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Hyperphosphatasia with intellectual disability syndrome Intellectual developmental disorder dysmorphic facial
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETD5(3)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. Cluster 337 →
Activated pi3k-delta syndrome Diffuse idiopathic skeletal hyperostosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIK3R1(2)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Central precocious puberty Estrogen resistance
1 gene
Show details
1 of 1 corroborated by 2+ sources
ESR1(6)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Cleidocranial dysplasia Diffuse idiopathic skeletal hyperostosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SUPT3H(2)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Benign mucous membrane pemphigoid with ocular involvement Congenital pulmonary artery atresia
1 gene
Show details
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. Cluster 1 →
Bouillaud’s disease Congenital pulmonary artery atresia
1 gene
Show details
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. Cluster 1 →
Central serous retinopathy Throat disease
1 gene
Show details
GATA5(1)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. Cluster 107 →
Heparin cofactor 2 deficiency Post-operative acute kidney injury
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF4G3(2)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
Arterial tortuosity syndrome Auditory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC2A10(7)
0.071 0.333 2.14e-3 3.04e-3 ✓ sig. —
atypical hemolytic-uremic syndrome with DGKE deficiency Hemolytic uremic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DGKE(5)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Benign mesial temporal lobe epilepsy Temporal lobe epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CPA6(3)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Cortical dysplasia-focal epilepsy syndrome Hyperkinesia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CNTNAP2(4)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Delpire-mcneill syndrome Temporal lobe epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC12A2(4)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Comp-related skeletal dysplasia Osteochondrodysplasias
1 gene
Show details
1 of 1 corroborated by 2+ sources
COMP(3)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Temporal lobe epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
NALCN(4)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —
Congenital limbs-face contractures-hypotonia-developmental delay syndrome Temporal lobe epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
NALCN(2)
0.029 1.000 2.14e-3 3.04e-3 ✓ sig. —

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