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
Carpenter syndrome MEGF8-related Carpenter syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MEGF8(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Carvajal syndrome Right ventricular cardiomyopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
DSP(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 201 →
Castleman disease Intracranial arteriovenous malformation
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 126 →
Cataract-alopecia-sclerodactyly syndrome Perniola krajewska carnevale syndrome
1 gene
Show details
LSS(1)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 362 →
Cataract-multisystem syndrome Dkc1-related disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
DKC1(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 64 →
Cataract-multisystem syndrome dyskeratosis congenita, x-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
DKC1(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 64 →
11p11.2 deletion syndrome Frontonasal dysplasia with alopecia and genital anomaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALX4(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
11p11.2 deletion syndrome Seizures, scoliosis, and macrocephaly/microcephaly syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXT2(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
11p11.2 deletion syndrome exostoses, multiple, type 2
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXT2(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
11p11.2 deletion syndrome Intellectual developmental disorder behavioral dysmorphic
1 gene
Show details
1 of 1 corroborated by 2+ sources
PHF21A(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
14q11.2 microduplication syndrome Chromodomain helicase dna binding protein 8 overgrowth syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHD8(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 279 →
14q11.2 microduplication syndrome FOXG1 disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
FOXG1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 279 →
17,20-lyase deficiency Malignant hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP17A1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
17q21.31 microdeletion syndrome Chromosome 17q21.31 deletion syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KANSL1(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
1p31p32 microdeletion syndrome Brain malformations
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFIA(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
3-hydroxyisobutyryl-coa hydrolase deficiency Beta-hydroxyisobutyryl-coa deacylase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
HIBCH(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
46, xy disorder of sex development NR5A1-related sex development disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR5A1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 38 →
Aapoai amyloidosis Ataxia with vitamin e deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOA1(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
ABCA4-related retinopathy Bietti crystalline corneoretinal dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCA4(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Abeta amyloidosis Amyloid neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
APP(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 116 →
Aceruloplasminemia Ferroxidase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CP(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 231 →
Achondrogenesis TRIP11-related skeletal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIP11(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 183 →
Achondrogenesis De la chapelle dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC26A2(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 183 →
Achondrogenesis Diastrophic dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC26A2(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 183 →
Achondrogenesis Diastrophic dysplasia, broad bone-platyspondylic variant
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC26A2(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 183 →

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