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
Thrombomodulin-related bleeding disorder Thrombophilia
1 gene
Show details
1 of 1 corroborated by 2+ sources
THBD(7)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 55 →
Thrombophilia thrombophilia, X-linked, due to factor 9 defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
F9(6)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Orofaciodigital syndrome TOPORS-related retinopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TOPORS(3)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Polyarticular juvenile idiopathic arthritis Tyrosine kinase 2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
TYK2(3)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Aplastic anemia Van esch-o’driscoll syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLA1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Aplastic anemia White blood cell count quantitative trait locus
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACKR1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 64 →
Aplastic anemia X-linked reticulate pigmentary disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLA1(5)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Ectodermal dysplasia Schopf-schulz-passarge syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
WNT10A(4)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Ectodermal dysplasia Sebaceous gland neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEF1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Ectodermal dysplasia Sebocystomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRT17(3)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Aplastic anemia Severe neonatal spondylometaphyseal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SBDS(4)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Aplastic anemia Short telomere syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACD(4)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 64 →
Shukla-vernon syndrome Wilms tumor
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCORL1(5)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 35 →
Heart defect, tongue hamartoma and polysyndactyly Orofaciodigital syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
WDPCP(4)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 8 →
Hemophilia a carriers Thrombophilia
1 gene
Show details
1 of 1 corroborated by 2+ sources
F8(5)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Hemophilia b carriers Thrombophilia
1 gene
Show details
1 of 1 corroborated by 2+ sources
F9(7)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Thrombophilia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HRG(4)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 55 →
hyper-IgE recurrent infection syndrome 5, autosomal recessive Polyarticular juvenile idiopathic arthritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6R(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
congenital myasthenic syndrome 2A Corneal dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHRNB1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
congenital myasthenic syndrome 2C Corneal dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHRNB1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Congenital prekallikrein deficiency Corneal dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
KLKB1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Congenital tufting enteropathy Hereditary breast cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPCAM(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Cornea plana Corneal dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
KERA(5)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
Coronary aneurysm Intellectual developmental disorder expressive speech dysmorphic
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETBP1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 271 →
Coronary aneurysm Schinzel-Giedion syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETBP1(2)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. Cluster 271 →

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