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
Brown oculocutaneous albinism oculocutaneous albinism type 2
1 gene
Show details
1 of 1 corroborated by 2+ sources
OCA2(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Bruton type agammaglobulinemia X-linked agammaglobulinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
BTK(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Bruton type agammaglobulinemia X-linked hypogammaglobulinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
BTK(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Bulbo-spinal atrophy, x-linked Partial androgen insensitivity syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
AR(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 193 →
Bulbo-spinal atrophy, x-linked Kennedy disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
AR(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 193 →
Bullous diffuse cutaneous mastocytosis Mast cell leukemia
1 gene
Show details
KIT(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 402 →
Bullous diffuse cutaneous mastocytosis Telangiectasia macularis eruptiva perstans
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIT(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 402 →
Bullous diffuse cutaneous mastocytosis Testicular seminoma
1 gene
Show details
KIT(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 402 →
Bullous diffuse cutaneous mastocytosis Urticaria pigmentosa
1 gene
Show details
KIT(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 402 →
Bullous pyoderma gangrenosum Pyoderma gangrenosum
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTPN6(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Burnett schwartz berberian syndrome Tricuspid atresia
1 gene
Show details
LRP1(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 194 →
Buschke-ollendorff syndrome Dermatofibrosis lenticularis disseminata
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEMD3(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 175 →
Buschke-ollendorff syndrome Osteopoikilosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEMD3(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 175 →
Butyrylcholinesterase deficiency Trismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCHE(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 378 →
Café-au-lait macules LZTR1-related schwannomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
LZTR1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Caffey disease Maternal hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL1A1(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 138 →
Caffey disease Rhizomelia
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL1A1(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 138 →
Caffey disease COL1A1-related Ehlers-Danlos syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL1A1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 138 →
Calvarial doughnut lesions with bone fragility Doughnut lesion of calvaria and bone fragility syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SGMS2(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Campomelic dysplasia Camptomelic dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOX9(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 310 →
Campomelic dysplasia Cooks syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOX9(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 310 →
Campomelic dysplasia isolated Pierre-Robin syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOX9(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 310 →
Camptodactyly, tall stature, and hearing loss syndrome Catshl syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR3(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 184 →
Camptodactyly, tall stature, and hearing loss syndrome Crouzon syndrome with acanthosis nigricans
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR3(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 184 →
Camptodactyly, tall stature, and hearing loss syndrome Muenke syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR3(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 184 →

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