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
Diabetic maculopathy neuroblastoma, susceptibility to, 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALK(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Diabetic maculopathy Turricephaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZIC1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Diazoxide-resistant focal hyperinsulinism due to kir6.2 deficiency Transient neonatal diabetes mellitus
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCNJ11(6)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency Transient neonatal diabetes mellitus
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCC8(7)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Cardiac conduction disease dilated cardiomyopathy 1EE
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH6(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Distal renal tubular acidosis renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
dystonia 27 Dystonia musculorum deformans
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL6A3(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Dystonia musculorum deformans GTP cyclohydrolase I deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GCH1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Early onset progressive leukoencephalopathy-central nervous system calcification-hearing loss-visual impairment syndrome Optic neuropathy
1 gene
Show details
KARS1(1)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Optic neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
KARS1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Congenital arteriovenous malformation EPHB4-associated vascular malformation spectrum
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPHB4(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Kabuki syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNMT3B(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 335 →
immunodeficiency-centromeric instability-facial anomalies syndrome 2 Kabuki syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZBTB24(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 335 →
Hepatic insufficiency immunodeficiency, developmental delay, and hypohomocysteinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFE2L2(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Imperforate anus Neurooculorenal syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ROBO1(4)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Imperforate anus Intellectual developmental disorder dysmorphic ocular microcephaly peripheral
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTNNB1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
inborn disorder of cobalamin metabolism and transport Intracellular cobalamin metabolism disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMADHC(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
interstitial lung disease due to ABCA3 deficiency Pulmonary alveolar proteinosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCA3(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Intrahepatic cholestasis mednik syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP1S1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 319 →
Intrahepatic cholestasis progressive familial intrahepatic cholestasis type 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCB4(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 319 →
Branchial arch abnormalities syndrome Kabuki syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KMT2D(8)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Branchial cleft anomalies Kabuki syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KMT2D(8)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Benign pemphigus P5CS deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Darier disease P5CS deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Optic neuropathy Periodic paralysis with later-onset distal motor neuropathy
1 gene
Show details
ATP8(1)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 32 →

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