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
COG5-congenital disorder of glycosylation Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
COG5(2)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia Van esch-o’driscoll syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLA1(2)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia X-linked reticulate pigmentary disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLA1(5)
0.001 1.000 7.01e-2 7.14e-2 —
fanconi anemia complementation group e Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
FANCE(2)
0.001 1.000 7.01e-2 7.14e-2 —
glutaryl-CoA dehydrogenase deficiency Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GCDH(2)
0.001 1.000 7.01e-2 7.14e-2 —
Congenital myelofibrosis with anemia Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
RBSN(3)
0.001 1.000 7.01e-2 7.14e-2 —
Craniolenticulosutural dysplasia Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SEC23A(6)
0.001 1.000 7.01e-2 7.14e-2 Cluster 2 →
Blepharophimosis intellectual disability syndrome Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
UBE3B(2)
0.001 1.000 7.01e-2 7.14e-2 —
C3hex olfactory ability Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
OR2J3(2)
0.001 1.000 7.01e-2 7.14e-2 —
Autoinflammation with pulmonary and cutaneous vasculitis Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HCK(4)
0.001 1.000 7.01e-2 7.14e-2 —
Autoinflammatory disease, systemic, with vasculitis Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
LYN(4)
0.001 1.000 7.01e-2 7.14e-2 —
BBS1-related ciliopathy Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
BBS1(2)
0.001 1.000 7.01e-2 7.14e-2 —
Benign familial pemphigus Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP2C1(2)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia myopathy caused by variation in POMGNT2
1 gene
Show details
1 of 1 corroborated by 2+ sources
POMGNT2(2)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia Oculocerebrodental syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIK3C2A(3)
0.001 1.000 7.01e-2 7.14e-2 Cluster 2 →
Insomnia Oculocerebrofacial syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
UBE3B(4)
0.001 1.000 7.01e-2 7.14e-2 —
immunodeficiency 23 Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PGM3(2)
0.001 1.000 7.01e-2 7.14e-2 —
Developmental delay with dysmorphic facies and brain anomalies Insomnia
1 gene
Show details
1 of 1 corroborated by 2+ sources
U2AF2(5)
0.001 1.000 7.01e-2 7.14e-2 —
Hypothyroidism Nephropathic cystinosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC66A1(2)
0.003 0.333 7.11e-2 7.25e-2 —
Oligodendroglioma Thyroid hemiagenesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS13C(2)
0.002 0.500 7.13e-2 7.27e-2 —
Mountain sickness Obstructive pulmonary disease
1 gene
Show details
AEBP2(1)
0.002 0.500 7.13e-2 7.27e-2 —
Attention deficit hyperactivity disorder mucopolysaccharidosis type 6
1 gene
Show details
1 of 1 corroborated by 2+ sources
ARSB(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Delayed sleep phase syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CRY1(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Cohen-gibson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EED(6)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder congenital disorder of glycosylation, type Iw, autosomal dominant
1 gene
Show details
1 of 1 corroborated by 2+ sources
STT3A(2)
0.001 1.000 7.18e-2 7.31e-2 —

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