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
Dend syndrome Hyperinsulinemic hypoglycemia
2 genes
Show details
2 of 2 corroborated by 2+ sources
ABCC8(5), KCNJ11(6)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. —
Melanocytic nevus Schimmelpenning-feuerstein-mims syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
NRAS(2), HRAS(2)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 18 →
Ataxia telangiectasia Chromosome 17q21.31 deletion syndrome
2 genes
Show details
1 of 2 corroborated by 2+ sources
ATM(7), C11orf65(1)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 348 →
Autoimmune lymphoproliferative disorder Schimmelpenning-feuerstein-mims syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
KRAS(2), NRAS(4)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 18 →
Bouillaud’s disease Cutaneous lupus erythematosus
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 1 →
Cutaneous lupus erythematosus Skeletal system disease
2 genes
Show details
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 1 →
Cutaneous lupus erythematosus Wheat allergic reaction
2 genes
Show details
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 1 →
Congenital fiber type disproportion myopathy Eichsfeld type congenital muscular dystrophy
2 genes
Show details
2 of 2 corroborated by 2+ sources
ACTA1(3), SELENON(4)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. —
Congenital fiber type disproportion myopathy Rigid spine muscular dystrophy
2 genes
Show details
2 of 2 corroborated by 2+ sources
ACTA1(4), SELENON(4)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. —
Congenital fiber type disproportion myopathy Multiminicore myopathy
2 genes
Show details
2 of 2 corroborated by 2+ sources
MYH7(2), SELENON(3)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. —
Anhydramnios autosomal recessive polycystic kidney disease
2 genes
Show details
2 of 2 corroborated by 2+ sources
PKD1(2), PKHD1(2)
0.154 0.667 1.39e-6 7.96e-6 ✓ sig. Cluster 157 →
Delirium Learning disorders
3 genes
Show details
3 of 3 corroborated by 2+ sources
IGF1(2), IL1RN(2), TH(2)
0.068 0.300 1.39e-6 7.97e-6 ✓ sig. —
Lymphedema Sinusitis
3 genes
Show details
1 of 3 corroborated by 2+ sources
HLA-DQA1(1), HLA-DRB1(1), MET(2)
0.083 0.188 1.40e-6 8.01e-6 ✓ sig. Cluster 1 →
Turner syndrome Ureteral calculi
2 genes
Show details
2 of 2 corroborated by 2+ sources
CAT(2), SOD1(2)
0.182 0.500 1.42e-6 8.09e-6 ✓ sig. Cluster 285 →
Autoimmune polyendocrine syndrome Obstructive asthma
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.182 0.500 1.42e-6 8.09e-6 ✓ sig. Cluster 1 →
Esophageal achalasia Obstructive asthma
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.182 0.500 1.42e-6 8.09e-6 ✓ sig. Cluster 1 →
Obstructive asthma Oropharyngeal neoplasms
2 genes
Show details
2 of 2 corroborated by 2+ sources
0.182 0.500 1.42e-6 8.09e-6 ✓ sig. Cluster 1 →
Cavernous malformations of cns Developmental venous anomaly
2 genes
Show details
PDCD10(1), CCM2(1)
0.182 0.500 1.42e-6 8.09e-6 ✓ sig. Cluster 308 →
Allergic contact dermatitis Contact dermatitis
6 genes
Show details
6 of 6 corroborated by 2+ sources
BCL2(2), TLR4(2), CYP1A1(2), IL18(2), CASP8(2), CCR1(2)
0.042 0.082 1.43e-6 8.18e-6 ✓ sig. Cluster 16 →
Amyloid polyneuropathy Amyloidosis
2 genes
Show details
2 of 2 corroborated by 2+ sources
APOA1(2), TTR(6)
0.100 1.000 1.44e-6 8.23e-6 ✓ sig. —
Aortic disease Brittle cornea syndrome
2 genes
Show details
2 of 2 corroborated by 2+ sources
PRDM5(7), ZNF469(7)
0.100 1.000 1.44e-6 8.23e-6 ✓ sig. —
Neuropathy Visual system disorder
2 genes
Show details
EFEMP1(1), PNPT1(1)
0.100 1.000 1.44e-6 8.23e-6 ✓ sig. Cluster 146 →
B-lymphoblastic leukemia/lymphoma Vulvar lichen sclerosus
2 genes
Show details
2 of 2 corroborated by 2+ sources
TP53(3), CDKN2A(3)
0.100 1.000 1.44e-6 8.23e-6 ✓ sig. Cluster 3 →
Ductal carcinoma of breast Lymphatic metastasis
3 genes
Show details
SOD2(1), ERBB2(1), CD274(1)
0.075 0.250 1.45e-6 8.28e-6 ✓ sig. —
Ectodermal dysplasia Tooth agenesis
4 genes
Show details
4 of 4 corroborated by 2+ sources
EDA(6), TSPEAR(4), WNT10A(8), EDARADD(6)
0.057 0.125 1.47e-6 8.40e-6 ✓ sig. —

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