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
Peritonitis Tuberous sclerosis complex
1 gene
Show details
1 of 1 corroborated by 2+ sources
IFNG(4)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Cold paroxysmal hemoglobinuria Peritonitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
C5(2)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Congenital hearing disorder hearing loss, autosomal recessive
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC22A4(2)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Absence epilepsy Synovial disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
GABRB3(2)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. Cluster 47 →
Cold paroxysmal hemoglobinuria Terminal complement component deficiency
1 gene
Show details
C5(1)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Hemoglobinuria paroxysmal Terminal complement component deficiency
1 gene
Show details
C5(1)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Cafe-au-lait spots Corticobasal degeneration
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOS1(2)
0.077 0.167 2.72e-3 3.66e-3 ✓ sig. —
Crisponi syndrome Esophageal ulcer
1 gene
Show details
1 of 1 corroborated by 2+ sources
CRLF1(5)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Bouillaud’s disease Fatigue syndrome
1 gene
Show details
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Bile acid malabsorption Intestinal disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC10A2(5)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Bicuspid aortic valve Throat disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA5(3)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Avascular necrosis of bone Torg-winchester syndrome
1 gene
Show details
MMP2(1)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Metabolic bone disorder Torg-winchester syndrome
1 gene
Show details
MMP2(1)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Partington syndrome X-linked syndromic complex neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP1S2(2)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Cold-induced sweating syndrome Esophageal ulcer
1 gene
Show details
1 of 1 corroborated by 2+ sources
CRLF1(5)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Congenital bone marrow failure syndrome Pancytopenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERCC6L2(5)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Cerebral artery occlusion Hyperemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADCYAP1(3)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Coronary restenosis Leukocyte adhesion deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITGB2(6)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Male infertility y chromosome microdeletion Spermatogenic failure, y-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
USP9Y(4)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Lymphoproliferative syndrome MHC class I deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
TAP2(2)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. —
Cleft palate and bilateral cleft lip Mitochondrial encephalopathy
1 gene
Show details
COX3(1)
0.059 0.333 2.73e-3 3.66e-3 ✓ sig. Cluster 32 →
Bladder exstrophy Vitreous body disease
1 gene
Show details
NCKAP5(1)
0.043 0.500 2.73e-3 3.66e-3 ✓ sig. —
Ataxia Parkinsonian-pyramidal syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SNCA(2)
0.043 0.500 2.73e-3 3.66e-3 ✓ sig. —
Hemorrhagic disease qualitative platelet defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBXA2R(3)
0.043 0.500 2.73e-3 3.66e-3 ✓ sig. Cluster 33 →
Ataxia Ophthalmoplegia
1 gene
Show details
1 of 1 corroborated by 2+ sources
NPC1(2)
0.043 0.500 2.73e-3 3.66e-3 ✓ sig. —

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