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
Delayed sleep phase syndrome Sleep disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
CRY1(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 177 →
Adrenocortical carcinoma Demyelinating diseases
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP53(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 3 →
Choroid plexus carcinoma Demyelinating diseases
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP53(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 3 →
Choroid plexus papilloma Demyelinating diseases
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP53(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 3 →
Erythrocyte lactate transporter defect Hyperinsulinemic hypoglycemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC16A1(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Factor vii deficiency Hematuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
F7(5)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Autoimmune lymphoproliferative disorder FAS-related autoimmune lymphoproliferative immune disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAS(7)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Fatty acid and ketone body metabolism disorder Hyperinsulinemic hypoglycemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC16A1(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Fatty acid oxidation and ketone body metabolism disorder Hyperinsulinemic hypoglycemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC16A1(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Cardiovascular abnormalities Gata2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA2(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 136 →
Gaucher disease due to saposin C deficiency Retinitis pigmentosa-deafness syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSAP(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 118 →
Genetic transient congenital hypothyroidism Idiopathic basal ganglia calcification
1 gene
Show details
1 of 1 corroborated by 2+ sources
DUOX2(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Cushing's disease Glucocorticoid receptor deficiency/resistance
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR3C1(5)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Combined psap deficiency Retinitis pigmentosa-deafness syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSAP(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 118 →
17,20-lyase deficiency Congenital adrenal hyperplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP17A1(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 346 →
Congenital adrenal hyperplasia Steroid 17-alpha-monooxygenase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP17A1(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. Cluster 346 →
Congenital adrenal hyperplasia Dosage-sensitive sex reversal
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR0B1(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital adrenal hyperplasia X-linked adrenal hypoplasia congenita
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR0B1(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital adrenal hyperplasia Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYP21A2(5)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital cataract anterior segment dysgenesis syndrome Posterior subcapsular cataract
1 gene
Show details
1 of 1 corroborated by 2+ sources
PITX3(2)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital factor vii deficiency Hematuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
F7(5)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital fiber type disproportion myopathy Congenital generalized hypercontractile muscle stiffness syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TPM3(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital hypoplasia of clavicle Posterior subcapsular cataract
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEMD2(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
Congenital adrenal hyperplasia Congenital lipoid adrenal hyperplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
STAR(4)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —
H syndrome Hypertrichosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC29A3(3)
0.083 1.000 7.14e-4 1.34e-3 ✓ sig. —

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