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
Nonobstructive azoospermia Schizophrenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC26A8(2)
0.000 1.000 1.65e-1 1.66e-1 —
Oculocerebrodental syndrome Schizophrenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIK3C2A(3)
0.000 1.000 1.65e-1 1.66e-1 Cluster 2 →
orofaciodigital syndrome type 14 Schizophrenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
C2CD3(2)
0.000 1.000 1.65e-1 1.66e-1 —
Nasopalpebral lipoma-coloboma syndrome Schizophrenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZDBF2(2)
0.000 1.000 1.65e-1 1.66e-1 —
optic atrophy 15 Schizophrenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
MCAT(2)
0.000 1.000 1.65e-1 1.66e-1 —
Bile duct disease Metabolic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FECH(3)
0.001 0.500 1.62e-1 1.63e-1 —
Auroneurodental syndrome Metabolic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HYAL3(2)
0.001 0.500 1.62e-1 1.63e-1 Cluster 2 →
Bipolar disorder Birk-aharoni syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSMC1(3)
0.001 0.500 1.52e-1 1.53e-1 Cluster 2 →
Intellectual developmental disorder Thiamine-responsive maple syrup urine disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
BCKDHA(2)
0.001 0.333 1.49e-1 1.50e-1 —
Atrichia with papular lesions Obesity
1 gene
Show details
1 of 1 corroborated by 2+ sources
HR(6)
0.001 0.500 1.49e-1 1.50e-1 —
Alzheimer disease nemaline myopathy 10
1 gene
Show details
1 of 1 corroborated by 2+ sources
LMOD3(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease optic atrophy 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
OPA3(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease glutamate pyruvate transaminase 2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GPT2(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Galactose mutarotase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GALM(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease FNIP1-associated syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FNIP1(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Intellectual developmental disorder dysmorphic cardiac
1 gene
Show details
1 of 1 corroborated by 2+ sources
TMEM94(4)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Intellectual developmental disorder dysmorphic ocular
1 gene
Show details
1 of 1 corroborated by 2+ sources
MTSS2(4)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease inflammatory skin and bowel disease, neonatal, 1
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADAM17(3)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease immunodeficiency 65, susceptibility to viral infections
1 gene
Show details
1 of 1 corroborated by 2+ sources
IRF9(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease polyglucosan body myopathy 1 with or without immunodeficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
RBCK1(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Pash syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NCSTN(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Pancreatic insufficiency syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COX4I2(4)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease Parkinsonism with polyneuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
UQCRC1(3)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease purine nucleoside phosphorylase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
PNP(2)
0.000 1.000 1.44e-1 1.45e-1 —
Alzheimer disease perrault syndrome 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLPP(2)
0.000 1.000 1.44e-1 1.45e-1 —

Showing 25 of 20825 pairs, sorted by significance (descending). Click a column header to sort.