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
Intellectual developmental disorder stankiewicz-isidor syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSMD12(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Richieri costa pereira syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF4A3(4)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder syndromic X-linked intellectual disability Raymond type
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZDHHC9(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder syndromic X-linked intellectual disability Siderius type
1 gene
Show details
1 of 1 corroborated by 2+ sources
PHF8(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Retinitis pigmentosa and erythrocytic microcytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRNT1(5)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder intellectual disability, autosomal recessive 61
1 gene
Show details
1 of 1 corroborated by 2+ sources
RUSC2(5)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Kidney atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder short stature facial speech
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBXL3(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder short stature facial
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBXL3(3)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder seizures epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
AP2M1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder seizures dysmorphic gait
1 gene
Show details
1 of 1 corroborated by 2+ sources
WDR26(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder peripheral neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
NUDT2(5)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Intellectual developmental disorder Intellectual developmental disorder growth microcephaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTCF(3)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder growth metabolic
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIP2B(4)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder dysmorphic seizures
1 gene
Show details
1 of 1 corroborated by 2+ sources
OTUD6B(5)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder dysmorphic ocular
1 gene
Show details
1 of 1 corroborated by 2+ sources
MTSS2(3)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Intellectual developmental disorder Intellectual developmental disorder dysmorphic hypotonia
1 gene
Show details
1 of 1 corroborated by 2+ sources
KMT5B(5)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Intellectual developmental disorder dysmorphic
1 gene
Show details
1 of 1 corroborated by 2+ sources
POU3F3(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Intellectual developmental disorder jaberi-elahi syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
GTPBP2(2)
0.001 1.000 5.25e-2 5.42e-2 —
Chondroblastoma Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
H3-3B(2)
0.001 1.000 5.25e-2 5.42e-2 —
Clark-baraitser syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIP12(4)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Chopra-amiel-gordon syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANKRD17(4)
0.001 1.000 5.25e-2 5.42e-2 —
Cimdag syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS4A(3)
0.001 1.000 5.25e-2 5.42e-2 —
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS4A(4)
0.001 1.000 5.25e-2 5.42e-2 —
Cerebrocostomandibular syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SNRPB(6)
0.001 1.000 5.25e-2 5.42e-2 —

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