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
Congenital retinal aneurysm Cyclin-dependent kinase-like 5 deficiency
1 gene
Show details
RS1(1)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital retinal anomaly Cyclin-dependent kinase-like 5 deficiency
1 gene
Show details
RS1(1)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital retrognathism kbg syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANKRD11(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital retrognathism Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCC8(3)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital retrognathism hyperinsulinemic hypoglycemia, familial, 1
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCC8(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital retrognathism Reynolds syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
LBR(5)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 280 →
Congenital sclerocornea Sutural cataract
1 gene
Show details
1 of 1 corroborated by 2+ sources
GJA8(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Congenital sensory neuropathy Skin ulcer
1 gene
Show details
1 of 1 corroborated by 2+ sources
NGF(3)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 330 →
Congenital thyroid atrophy Interrupted aortic arch
1 gene
Show details
NKX2-5(1)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Bethlem myopathy Congenital-onset steinert myotonic dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
DMPK(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Cardiac valvular dysplasia Conjunctival telangiectasis
1 gene
Show details
ATM(1)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contracture of multiple joints dystonia 27
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL6A3(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contracture of multiple joints Schaaf-yang syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MAGEL2(5)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contracture of multiple joints lethal congenital contracture syndrome 11
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLDN(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contracture of multiple joints Encephaloclastic proliferative vasculopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
FLVCR2(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contractures, pterygia, and spondylocarpotarsal fusion syndrome Digitotalar dysmorphism
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH3(4)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Contractures, pterygia, and variable skeletal fusions syndrome Digitotalar dysmorphism
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH3(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Cryptogenic multifocal ulcerous stenosing enteritis Curling ulcer
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLA2G4A(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 265 →
Curling ulcer Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLA2G4A(5)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 265 →
Curling ulcer Urinary bladder neck obstruction
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTGS2(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
CYP1B1-related glaucoma with or without anterior segment dysgenesis Hydrophthalmos
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP1B1(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Cytochrome-b5 reductase deficiency Methemoglobinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYB5R3(6)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Dacryocystitis Exanthema
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL1RN(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 216 →
Deafness-lymphedema-leukemia syndrome Vascular remodeling
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA2(3)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 136 →
Erythropoietic protoporphyria X-linked erythropoietic protoporphyria
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALAS2(7)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. Cluster 158 →

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