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
Congenital central hypothyroidism Monoclonal b-cell lymphocytosis
1 gene
Show details
IRS4(1)
0.077 0.500 1.42e-3 2.04e-3 ✓ sig. —
Intellectual developmental disorder seizures language Monoclonal b-cell lymphocytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SETD1B(4)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Intellectual developmental disorder, autosomal dominant 47 Monoclonal b-cell lymphocytosis
1 gene
Show details
STAG1(1)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Intellectual disability, epilepsy and autism Monoclonal b-cell lymphocytosis
1 gene
Show details
SETD1B(1)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Mental retardation, autosomal dominant 47 Monoclonal b-cell lymphocytosis
1 gene
Show details
STAG1(1)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Limb, scalp and skull defects Monoclonal b-cell lymphocytosis
1 gene
Show details
NOTCH1(1)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Monoclonal b-cell lymphocytosis Pituitary adenoma 4, adrenocorticotropic hormone-secreting
1 gene
Show details
USP8(1)
0.083 1.000 7.10e-4 1.17e-3 ✓ sig. —
Blue nevus Monoclonal b-cell lymphocytosis
2 genes
Show details
NOTCH1(1), SF3B1(1)
0.083 0.182 4.15e-5 1.98e-4 ✓ sig. —

Showing 8 of 8 matching pairs, sorted by significance (descending). Click a column header to sort.