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
Acetyl-coa carboxylase deficiency Erectile dysfunction
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACACA(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Autoinflammatory syndrome, familial, behcet-like Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TNFAIP3(5)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. Cluster 25 →
autosomal systemic lupus erythematosus type 16 Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. Cluster 25 →
myopathy, proximal, and ophthalmoplegia Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH2(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLS(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease Interleukin 6 quantitative trait
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6R(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease karyomegalic interstitial nephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAN1(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Congenital brain dysgenesis due to glutamine synthetase deficiency Huntington disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLUL(5)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. Cluster 57 →
fibrodysplasia ossificans progressiva Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACVR1(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Gastroschisis Huntington disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADD1(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome Pulmonary hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
GBA1(4)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Glutaminase deficiency Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLS(4)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Borderline personality disorder Pulmonary hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
TPH1(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Casgid syndrome Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
GLS(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease hyper-IgE recurrent infection syndrome 5, autosomal recessive
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL6R(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Cerebellar-facial-dental syndrome Huntington disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
BRF1(6)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYH2(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Chromosome 5q12 deletion syndrome Myositis
1 gene
Show details
1 of 1 corroborated by 2+ sources
PDE4D(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Myositis Separation anxiety disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
DRD4(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Myositis spinocerebellar ataxia, autosomal recessive 25
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATG5(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. Cluster 25 →
Erectile dysfunction Multiple intestinal atresia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TTC7A(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Pulmonary hypertension pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF2AK4(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Atypical femoral fracture Nasal polyp
2 genes
Show details
IL18R1(1), SLC9A4(1)
0.027 0.054 3.94e-3 4.99e-3 ✓ sig. —
Color vision deficiency Ear disorder
2 genes
Show details
SCML4(1), COL26A1(1)
0.002 1.000 3.93e-3 4.99e-3 ✓ sig. Cluster 2 →
Martsolf syndrome Parenchymal hematoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
SEMA3A(2)
0.063 0.167 3.89e-3 4.94e-3 ✓ sig. —

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