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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.
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Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▲ Shared cluster
mucopolysaccharidosis type 9 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
HYAL1(2)
0.000 1.000 1.65e-1 1.66e-1 —
multiple congenital anomalies-hypotonia-seizures syndrome 1 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
PIGN(2)
0.000 1.000 1.65e-1 1.66e-1 —
Congenital cranial dysinnervation disorder Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
NEUROG1(3)
0.000 1.000 1.65e-1 1.66e-1 —
congenital disorder of glycosylation, type 2v Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
EDEM3(2)
0.000 1.000 1.65e-1 1.66e-1 —
Congenital hypotonia, epilepsy, developmental delay, and digital anomalies Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ATN1(4)
0.000 1.000 1.65e-1 1.66e-1 —
Congenital intrinsic factor deficiency Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
CBLIF(3)
0.000 1.000 1.65e-1 1.66e-1 —
ALG12-congenital disorder of glycosylation Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ALG12(2)
0.000 1.000 1.65e-1 1.66e-1 —
immunodeficiency 23 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
PGM3(2)
0.000 1.000 1.65e-1 1.66e-1 —
inflammatory bowel disease 28 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
IL10RA(2)
0.000 1.000 1.65e-1 1.66e-1 —
intellectual disability, autosomal recessive 61 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
RUSC2(2)
0.000 1.000 1.65e-1 1.66e-1 —
retinitis pigmentosa 86 Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
0.000 1.000 1.65e-1 1.66e-1 —
Schizophrenia SNRNP200-related dominant retinopathy
1 gene
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1 of 1 corroborated by 2+ sources
0.000 1.000 1.65e-1 1.66e-1 —
Schizophrenia spinocerebellar ataxia, autosomal recessive 23
1 gene
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1 of 1 corroborated by 2+ sources
TDP2(2)
0.000 1.000 1.65e-1 1.66e-1 —
Schizophrenia spondyloepimetaphyseal dysplasia with joint laxity, type 3
1 gene
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1 of 1 corroborated by 2+ sources
EXOC6B(2)
0.000 1.000 1.65e-1 1.66e-1 —
Schizophrenia sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2
1 gene
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1 of 1 corroborated by 2+ sources
MOCS3(2)
0.000 1.000 1.65e-1 1.66e-1 —
Early-onset dystonia with spastic paraplegia Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ATP5MC3(5)
0.000 1.000 1.65e-1 1.66e-1 —
Catatonia Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
CHRM4(2)
0.000 1.000 1.65e-1 1.66e-1 —
Cayman type cerebellar ataxia Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ATCAY(2)
0.000 1.000 1.65e-1 1.66e-1 —
Cednik syndrome Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
SNAP29(4)
0.000 1.000 1.65e-1 1.66e-1 —
Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
SNAP29(3)
0.000 1.000 1.65e-1 1.66e-1 —
Charcot-Marie-Tooth disease, axonal, type 2FF Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
CADM3(2)
0.000 1.000 1.65e-1 1.66e-1 —
Childhood-onset dystonia Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
MECR(2)
0.000 1.000 1.65e-1 1.66e-1 —
Childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
MECR(5)
0.000 1.000 1.65e-1 1.66e-1 —
Corneal injury Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ALDH3A1(2)
0.000 1.000 1.65e-1 1.66e-1 —
Dentatorubral pallidoluysian atrophy Schizophrenia
1 gene
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1 of 1 corroborated by 2+ sources
ATN1(6)
0.000 1.000 1.65e-1 1.66e-1 —

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