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
Intracellular cobalamin metabolism disorder methylcobalamin deficiency type cblG
1 gene
Show details
1 of 1 corroborated by 2+ sources
MTR(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Intracellular cobalamin metabolism disorder methylmalonic acidemia with homocystinuria, type cblJ
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCD4(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. Cluster 246 →
Intracellular cobalamin metabolism disorder methylmalonic aciduria and homocystinuria type cblF
1 gene
Show details
1 of 1 corroborated by 2+ sources
LMBRD1(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Microcephalic dwarfism Polycythemia vera
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNMT3A(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Hepatic insufficiency Mucocutaneous ulceration
1 gene
Show details
1 of 1 corroborated by 2+ sources
RELA(3)
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. —
Developmental delay with immunodeficiency syndrome Hepatic insufficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFE2L2(3)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
Diabetic maculopathy hao-fountain syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
USP7(2)
0.100 1.000 5.84e-4 1.16e-3 ✓ sig. —
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. —

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