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
hearing loss, X-linked 6 Leiomyoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL4A6(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 49 →
Heme oxygenase deficiency Vascular system injury
1 gene
Show details
1 of 1 corroborated by 2+ sources
HMOX1(7)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 371 →
Hengel maroofian schols syndrome Ureterolithiasis
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCAS3(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Hepatoerythropoietic porphyria Porphyria
1 gene
Show details
1 of 1 corroborated by 2+ sources
UROD(6)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
hereditary spherocytosis Spherocytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANK1(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 168 →
Deep vein thrombosis hereditary thrombophilia due to congenital protein C deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
PROC(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Dwarfism heyn-sproul-jackson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNMT3A(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
hyperinsulinemic hypoglycemia, familial, 2 monogenic diabetes
1 gene
Show details
KCNJ11(1)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Hyperthermia Iron deficiency anemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GPX1(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 227 →
Hypochromic anemia Iron deficiency anemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC11A2(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 227 →
hypogonadotropic hypogonadism 1 with or without anosmia Martsolf syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANOS1(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
hypogonadotropic hypogonadism 3 with or without anosmia Septo-optic dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PROKR2(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 218 →
hypoinsulinemic hypoglycemia and body hemihypertrophy Partial lipodystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
AKT2(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Hypophosphatasia Ureterolithiasis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALPL(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Deep vein thrombosis hypoplasminogenemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLG(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Congenital muscular hypertrophy-cerebral syndrome Cornelia de lange syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMC1A(5)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 297 →
congenital myasthenic syndrome 17 Tooth abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
LRP4(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Acro-dermo-ungual-lacrimal-tooth syndrome Congenital skin anomaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Contracture Hyaline fibromatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANTXR2(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Cortical dysgenesis with pontocerebellar hypoplasia Martsolf syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TUBB3(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Craniodiaphyseal dysplasia IFT140-related recessive ciliopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
IFT140(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
craniofacial dysplasia - osteopenia syndrome Facial dysmorphism syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
IRX5(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Brachycephaly craniosynostosis 6
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZIC1(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Cutaneous polyarteritis nodosa Leiomyoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMAD3(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Dermatopathia pigmentosa reticularis Tongue neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRT14(6)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 269 →

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