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
Bile duct disorder Hypertensive heart disease
1 gene
Show details
PRKAG2(1)
0.063 0.167 3.89e-3 4.94e-3 ✓ sig. —
Tricuspid valve disease Trigeminal nerve disease
1 gene
Show details
KIF26B(1)
0.063 0.167 3.89e-3 4.94e-3 ✓ sig. —
Angelman syndrome Synovial disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
GABRB3(3)
0.063 0.167 3.89e-3 4.94e-3 ✓ sig. —
Childhood absence epilepsy Synovial disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
GABRB3(4)
0.063 0.167 3.89e-3 4.94e-3 ✓ sig. Cluster 47 →
Autosomal recessive ataxia Coenzyme q10 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
COQ8A(7)
0.059 0.200 3.89e-3 4.94e-3 ✓ sig. —
Frontotemporal dementia with or without amyotrophic lateral sclerosis Paraplegia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPG7(2)
0.059 0.200 3.89e-3 4.94e-3 ✓ sig. —
Cholecystitis Upper extremity fracture
1 gene
Show details
0.059 0.200 3.89e-3 4.94e-3 ✓ sig. —
Coloboma complex neurodevelopmental disorder with or without congenital anomalies
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH10(2)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Congenital mirror movements Hereditary breast and ovarian cancer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RAD51(2)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Gastro-entero-pancreatic neuroendocrine tumor MHC class II deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CIITA(2)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Hereditary breast and ovarian cancer syndrome Mirror movements
1 gene
Show details
1 of 1 corroborated by 2+ sources
RAD51(6)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Glycinuria with/without oxalate urolithiasis Macular telangiectasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC6A20(2)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Autoimmune nervous system disorder Gastro-entero-pancreatic neuroendocrine tumor
1 gene
Show details
1 of 1 corroborated by 2+ sources
EOMES(2)
0.053 0.250 3.89e-3 4.94e-3 ✓ sig. —
Pseudo-torch syndrome Splenomegaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
OCLN(6)
0.043 0.333 3.89e-3 4.94e-3 ✓ sig. —
Antiphospholipid syndrome Hepatitis c induced liver cirrhosis
1 gene
Show details
HLA-DRA(1)
0.043 0.333 3.89e-3 4.94e-3 ✓ sig. Cluster 1 →
Bulimia Congenital palmoplantar and perioral keratoderma of olmsted
1 gene
Show details
1 of 1 corroborated by 2+ sources
PERP(2)
0.043 0.333 3.89e-3 4.94e-3 ✓ sig. —
Bulimia Olmsted syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PERP(5)
0.043 0.333 3.89e-3 4.94e-3 ✓ sig. —
Burn-mckeown syndrome Hypomyelinating leukodystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLR1A(5)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. —
Dubowitz syndrome Spondylosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
LIG4(3)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. —
Multiple system atrophy Rib fracture
1 gene
Show details
TENM2(1)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. Cluster 207 →
Congenital cartilage disorder Smith-mccort dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYM(6)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. —
Cerebellar atrophy Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TYROBP(5)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. —
Lig4 syndrome Spondylosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
LIG4(5)
0.031 0.500 3.89e-3 4.94e-3 ✓ sig. —
Frontotemporal dementia leukoencephalopathy, diffuse hereditary, with spheroids 1
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSF1R(2)
0.016 1.000 3.90e-3 4.94e-3 ✓ sig. —
lysinuric protein intolerance Oropharyngeal cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC7A7(2)
0.016 1.000 3.90e-3 4.94e-3 ✓ sig. —

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