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
Coronary artery disease Thrombocytopenia with anemia and myelofibrosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MPIG6B(6)
0.001 1.000 7.42e-2 7.55e-2 —
Coronary artery disease TMEM165-congenital disorder of glycosylation
1 gene
Show details
1 of 1 corroborated by 2+ sources
TMEM165(2)
0.001 1.000 7.42e-2 7.55e-2 —
Coronary artery disease tooth agenesis, selective, 9
1 gene
Show details
1 of 1 corroborated by 2+ sources
GREM2(2)
0.001 1.000 7.42e-2 7.55e-2 —
Coronary artery disease VPS11-related neurological disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS11(2)
0.001 1.000 7.42e-2 7.55e-2 —
Coronary artery disease immunodeficiency 126, susceptibility to
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTCRA(2)
0.001 1.000 7.42e-2 7.55e-2 —
Coronary artery disease Intellectual developmental disorder growth metabolic
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIP2B(3)
0.001 1.000 7.42e-2 7.55e-2 Cluster 78 →
Hypertension immunodeficiency-centromeric instability-facial anomalies syndrome 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
HELLS(2)
0.001 1.000 7.46e-2 7.59e-2 —
fanconi anemia complementation group l Hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
FANCL(2)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension Primary hypomagnesemia with hypocalciuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
FXYD2(3)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension LIPE-related familial partial lipodystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
LIPE(2)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension MPI-congenital disorder of glycosylation
1 gene
Show details
1 of 1 corroborated by 2+ sources
MPI(2)
0.001 1.000 7.46e-2 7.59e-2 —
Congenital arthrogryposis with anterior horn cell disease Hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLE1(3)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension opsismodysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
INPPL1(3)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension Urocanate hydratase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
UROC1(8)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension Wernicke encephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TKT(3)
0.001 1.000 7.46e-2 7.59e-2 —
Arthrogryposis with anterior horn cell disease Hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLE1(2)
0.001 1.000 7.46e-2 7.59e-2 —
Autoinflammatory disease, systemic, with vasculitis Hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
LYN(4)
0.001 1.000 7.46e-2 7.59e-2 —
Hypertension renal hypomagnesemia 2
1 gene
Show details
1 of 1 corroborated by 2+ sources
FXYD2(3)
0.001 1.000 7.46e-2 7.59e-2 —
Birk-aharoni syndrome Dementia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSMC1(3)
0.002 0.500 7.52e-2 7.64e-2 Cluster 2 →
Acral peeling skin syndrome Glioblastoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSTA(2)
0.002 0.500 7.73e-2 7.86e-2 —
Androgenetic alopecia Thiamine-responsive maple syrup urine disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCKDHA(2)
0.002 0.333 7.74e-2 7.87e-2 —
Obesity White blood cell count quantitative trait locus
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACKR1(2)
0.001 1.000 7.75e-2 7.87e-2 —
Combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia Obesity
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACP5(2)
0.001 1.000 7.75e-2 7.87e-2 —
congenital disorder of glycosylation with defective fucosylation 2 Obesity
1 gene
Show details
1 of 1 corroborated by 2+ sources
FCSK(2)
0.001 1.000 7.75e-2 7.87e-2 —
congenital disorder of glycosylation, type 2v Obesity
1 gene
Show details
1 of 1 corroborated by 2+ sources
EDEM3(2)
0.001 1.000 7.75e-2 7.87e-2 —

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