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
Amyloid polyneuropathy Dystransthyretinemic euthyroidal hyperthyroxinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TTR(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 182 →
Amyloid polyneuropathy Senile systemic amyloidosis
1 gene
Show details
TTR(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 182 →
Amyloid polyneuropathy Transthyretin amyloid cardiomyopathy
1 gene
Show details
TTR(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 182 →
amyotrophic lateral sclerosis 26 with or without frontotemporal dementia Welander distal myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TIA1(5)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
amyotrophic lateral sclerosis type 10 Masp2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
TARDBP(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
amyotrophic lateral sclerosis type 11 Yunis-varon syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FIG4(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 103 →
amyotrophic lateral sclerosis type 19 Soft tissue neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERBB4(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Anaplastic astrocytoma Hairy cell leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
BRAF(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Anaplastic astrocytoma Anaplastic oligoastrocytoma
1 gene
Show details
IDH2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 304 →
Anaplastic astrocytoma Gemistocytic astrocytoma
1 gene
Show details
IDH2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 304 →
Anaplastic oligoastrocytoma Anaplastic oligodendroglioma
1 gene
Show details
IDH2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 304 →
Anaplastic oligodendroglioma Gemistocytic astrocytoma
1 gene
Show details
IDH2(1)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 304 →
Anaplastic oligodendroglioma Congenital chromosomal disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
POT1(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 304 →
Anaptoglobinemia Wilson disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP7B(6)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Andersen-tawil syndrome familial hyperaldosteronism type III
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCNJ5(3)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
Androgen insensitivity syndrome Bulbo-spinal atrophy, x-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
AR(7)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 193 →
Androgen insensitivity syndrome Partial androgen insensitivity syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
AR(7)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 193 →
Androgen insensitivity syndrome Kennedy disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
AR(8)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 193 →
Androgen insensitivity syndrome meier-gorlin syndrome 7
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDC45(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 193 →
anemia, nonspherocytic hemolytic, due to G6PD deficiency Anhidrotic ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema
1 gene
Show details
1 of 1 corroborated by 2+ sources
G6PD(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 87 →
anemia, nonspherocytic hemolytic, due to G6PD deficiency Autoinflammatory disease, systemic, x-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
G6PD(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 87 →
anemia, nonspherocytic hemolytic, due to G6PD deficiency Bloch sulzberger syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
G6PD(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 87 →
Anemia, x-linked Congenital erythropoietic porphyria
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA1(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 125 →
Anemia, x-linked Cutaneous porphyria
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA1(4)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 125 →
Anhidrotic ectodermal dysplasia X-linked hypohidrotic ectodermal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
EDA(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 117 →

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