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
Sitosterolemia Xanthomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCG5(7)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Aphasia Spinal cord compression
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLAT(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Postictal aphasia Spinal cord compression
1 gene
Show details
PLAT(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Cholesterol embolism Spinal cord compression
1 gene
Show details
PLAT(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Sweat gland disease Vipoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
SST(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 270 →
Hemimelia of limb Synpolydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
HOXD13(5)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 397 →
14q11.2 microduplication syndrome Intellectual developmental disorder autism dysmorphic
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHD8(5)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 279 →
17p11.2 microduplication syndrome Smith-magenis syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RAI1(7)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 347 →
17q12 microdeletion syndrome Renal cysts and diabetes syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HNF1B(7)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 23 →
1p36.33 duplication syndrome Ocular anomalies with axonal neuropathy and developmental delay
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATAD3A(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Acne inversa Early onset alzheimers disease with behavioral disturbance
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSEN1(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 116 →
Acrocallosal syndrome White sutton syndrome
1 gene
Show details
GLI3(1)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 142 →
Adrenoleukodystrophy Encephalitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ABCD1(4)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Alagille syndrome Corneal opacity
1 gene
Show details
1 of 1 corroborated by 2+ sources
JAG1(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 356 →
Alpha-1 antichymotrypsin deficiency Rh deficiency syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RHD(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 302 →
Anastomosing haemangioma Cutis marmorata telangiectatica congenita
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNA11(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 40 →
Anastomosing haemangioma Port-wine stain
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNAQ(3)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 40 →
Activated pi3k-delta syndrome Anisometropia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTEN(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Anisometropia Retinal vasculopathy with cerebral leukodystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTEN(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Annular epidermolytic ichthyosis Epidermolytic palmoplantar keratoderma
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRT1(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 230 →
Antithrombin deficiency Pyogenic arthritis-pyoderma gangrenosum-acne syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL1B(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —
Antithrombin deficiency Diffuse panbronchiolitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MUC5B(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 197 →
Antley-bixler syndrome Congenital aural atresia
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(6)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 85 →
Aplasia cutis congenita with epibulbar dermoids Arteriovenous malformations
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRAS(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. Cluster 40 →
Aplasia cutis congenita with epibulbar dermoids Encephalocraniocutaneous lipomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRAS(2)
0.200 0.500 3.90e-4 8.67e-4 ✓ sig. —

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