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
amyotrophic lateral sclerosis type 12 glaucoma, normal tension, susceptibility to
1 gene
Show details
OPTN(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
amyotrophic lateral sclerosis type 22 autosomal dominant macrothrombocytopenia
1 gene
Show details
TUBA4A(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
amyotrophic lateral sclerosis, susceptibility to, 25 inherited neurodegenerative disorder
1 gene
Show details
KIF5A(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Analbuminemia Blood protein disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 372 →
Analbuminemia Congenital analbuminemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 372 →
Analbuminemia Dysalbuminemic hyperthyroxinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALB(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 372 →
Anaphylatoxin inactivator deficiency Carboxypeptidase n deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CPN1(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Anaplastic oligoastrocytoma Gemistocytic astrocytoma
1 gene
Show details
IDH2(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 304 →
anemia, nonspherocytic hemolytic, due to G6PD deficiency G6PD deficiency
1 gene
Show details
G6PD(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 87 →
Anemia, x-linked Thrombocytopenia with dyserythropoietic anemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA1(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 125 →
Anemia, x-linked Dyserythropoietic anemia with abnormal platelets and neutropenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA1(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 125 →
Anemia, x-linked GATA1-Related X-Linked Cytopenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 125 →
Angiofollicular ganglionic hyperplasia Angiolymphoid hyperplasia
1 gene
Show details
IL6(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 126 →
Angiofollicular ganglionic hyperplasia Castleman disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 126 →
Angiolymphoid hyperplasia Castleman disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 126 →
Ankyloblepharon-ectodermal defects-cleft lip/palate Limb-mammary syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 27 →
Ankyloblepharon-ectodermal defects-cleft lip/palate Rudiger syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 27 →
Ankyloblepharon-ectodermal defects-cleft lip/palate Sweat gland neoplasm
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 27 →
Ankylosis Beare-stevenson cutis gyrata syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 85 →
Ankylosis Cutis gyrata syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR2(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 85 →
Anomalous pulmonary venous Deafness with cataract, intellectual disability, and polyneuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSMC3(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Anterior compartment syndrome Heme oxygenase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
HMOX1(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 371 →
Anterior maxillary protrusion-strabismus-intellectual disability syndrome Intellectual disability, anterior maxillary protrusion, and strabismus
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOBP(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Anterior pituitary function deficiency with variable immunodeficiency immunodeficiency, common variable, 10
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFKB2(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
anterior segment dysgenesis 4 Ring dermoid of cornea
1 gene
Show details
1 of 1 corroborated by 2+ sources
PITX2(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 253 →

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