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
Body weight TFAP2B-related congenital heart disease spectrum disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TFAP2B(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Patent ductus arteriosus TFAP2B-related congenital heart disease spectrum disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TFAP2B(5)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Hemophilia a thrombophilia, X-linked, due to factor 9 defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
F9(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Congenital anomaly of limb Timothy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CACNA1C(6)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Dentinogenesis imperfecta Tricho-dento-osseous syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DLX3(6)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Distal arthrogryposis Trismus-pseudocamptodactyly syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH8(4)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Catalepsy Tyrosine hydroxylase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
TH(4)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Pheochromocytoma Tyrosine hydroxylase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
TH(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Congenital anomaly of limb Ulnar-mammary syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBX3(6)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Vacterl association Vacterl-hydrocephalus syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FANCB(6)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Vacterl association Waardenburg anophthalmia syndrome
1 gene
Show details
SMOC1(1)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. Cluster 249 →
Congenital total cataract Wormian bones-micrognathia-abnormal dentition-progeroid syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEMD2(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Rett syndrome X-linked retinoschisis
1 gene
Show details
1 of 1 corroborated by 2+ sources
RS1(4)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Hydrops fetalis Yellow nail syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CELSR1(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Walker-warburg syndrome Yellow nail syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CELSR1(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Developmental disorder Riddle syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNF168(7)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Developmental disorder immunodeficiency, common variable, 10
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFKB2(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Diffuse gastric adenocarcinoma severe combined immunodeficiency due to LAT deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
LAT(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. Cluster 265 →
Congenital fibrosis of extraocular muscles Diffuse gastric and lobular breast cancer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTNNA1(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Disorder of sex development Primary aldosteronism
1 gene
Show details
1 of 1 corroborated by 2+ sources
RXFP2(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. Cluster 143 →
Body weight dyskeratosis congenita, autosomal recessive 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
WRAP53(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Dyskinesia, limb and orofacial, infantile-onset Thyroiditis
1 gene
Show details
1 of 1 corroborated by 2+ sources
PDE10A(4)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
ectodermal dysplasia and immunodeficiency 2 Gliosarcoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFKBIA(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
Dentinogenesis imperfecta Enamel-renal syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAM20A(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. Cluster 366 →
Encephaloclastic proliferative vasculopathy Hydrops fetalis
1 gene
Show details
1 of 1 corroborated by 2+ sources
FLVCR2(2)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —

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