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
Cardiac conduction disease MYH-6 related congenital heart defects
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH6(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Myoclonus-renal failure syndrome progressive myoclonus epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SCARB2(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 329 →
Cataract-microcornea syndrome nance-horan syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NHS(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 43 →
Epilepsy of infancy with migrating focal seizures neonatal encephalopathy with non-epileptic myoclonus
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCNQ2(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Neonatal hyperbilirubinemia Small cell carcinoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
UGT1A1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Crigler-najjar syndrome Neonatal hyperbilirubinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
UGT1A1(6)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Lucey-driscoll syndrome Neonatal hyperbilirubinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
UGT1A1(3)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Epilepsy of infancy with migrating focal seizures neonatal-onset developmental and epileptic encephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCNQ2(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Neurooculorenal syndrome Pituitary hormone deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ROBO1(5)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Nocturnal frontal lobe epilepsy primary ciliary dyskinesia 28
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPAG1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
normophosphatemic familial tumoral calcinosis Urogenital abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
SAMD9(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Exudative vitreoretinopathy norrie disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
NDP(5)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Hyperproinsulinemia obsolete early infantile epileptic encephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
GAD1(3)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 325 →
Aniridia Ocular dysgenesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ELP4(6)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 35 →
Diabetic polyneuropathy Other specified diabetes mellitus with unspecified complications
1 gene
Show details
1 of 1 corroborated by 2+ sources
WFS1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
16p13.2 microdeletion syndrome Diabetic maculopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
USP7(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
22q11.2 deletion syndrome Intermittent explosive disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
COMT(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
22q11.2 deletion syndrome Chromosome 22q11.2 microduplication syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBX1(3)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
22q11.2 deletion syndrome Conotruncal anomaly face syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBX1(3)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
8q24.3 microdeletion syndrome Charge syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PUF60(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 224 →
Aarskog-scott syndrome, x-linked Urogenital abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGD1(4)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Acral self-healing collodion baby Congenital ichthyosiform erythroderma
1 gene
Show details
1 of 1 corroborated by 2+ sources
TGM1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 233 →
Acrokeratosis verruciformis Darier disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP2A2(6)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
amyotrophic lateral sclerosis type 19 Peritoneal disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERBB4(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Aplasia and myelodysplasia Bone marrow failure syndromes
1 gene
Show details
1 of 1 corroborated by 2+ sources
SRP72(4)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 3 →

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