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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
Attention deficit hyperactivity disorder cardiomyopathy, dilated, 2j
1 gene
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1 of 1 corroborated by 2+ sources
FLII(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Blepharospasm
1 gene
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1 of 1 corroborated by 2+ sources
DRD5(3)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder primary ciliary dyskinesia 32
1 gene
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1 of 1 corroborated by 2+ sources
RSPH3(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder mucopolysaccharidosis type 6
1 gene
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1 of 1 corroborated by 2+ sources
ARSB(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Cerebral arterial disease
1 gene
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ADGRE3(1)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Diffuse cerebral and cerebellar atrophy–intractable seizures–progressive microcephaly syndrome
1 gene
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1 of 1 corroborated by 2+ sources
QARS1(4)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Delayed sleep phase syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CRY1(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Intellectual developmental disorder behavioral short stature
1 gene
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1 of 1 corroborated by 2+ sources
PUS7(4)
0.001 1.000 7.18e-2 7.31e-2 —
Al kaissi syndrome Attention deficit hyperactivity disorder
1 gene
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CDK10(1)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Cohen-gibson syndrome
1 gene
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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
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1 of 1 corroborated by 2+ sources
STT3A(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Bilateral cleft lip
1 gene
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1 of 1 corroborated by 2+ sources
PLEKHA5(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Benign essential blepharospasm
1 gene
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1 of 1 corroborated by 2+ sources
DRD5(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder STT3A-congenital disorder of glycosylation
1 gene
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1 of 1 corroborated by 2+ sources
STT3A(2)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder retinitis pigmentosa 18
1 gene
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1 of 1 corroborated by 2+ sources
PRPF3(2)
0.001 1.000 7.18e-2 7.31e-2 Cluster 2 →
Attention deficit hyperactivity disorder X-linked ichthyosis with steryl-sulfatase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
STS(3)
0.001 1.000 7.18e-2 7.31e-2 —
Attention deficit hyperactivity disorder Young syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CFAP221(3)
0.001 1.000 7.18e-2 7.31e-2 —
Oligodendroglioma Thyroid hemiagenesis
1 gene
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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
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AEBP2(1)
0.002 0.500 7.13e-2 7.27e-2 —
Hypothyroidism Nephropathic cystinosis
1 gene
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1 of 1 corroborated by 2+ sources
SLC66A1(2)
0.003 0.333 7.11e-2 7.25e-2 —
Insomnia myopathy caused by variation in POMGNT2
1 gene
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1 of 1 corroborated by 2+ sources
POMGNT2(2)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia Oculocerebrodental syndrome
1 gene
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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
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1 of 1 corroborated by 2+ sources
UBE3B(4)
0.001 1.000 7.01e-2 7.14e-2 —
Insomnia Van esch-o’driscoll syndrome
1 gene
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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
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1 of 1 corroborated by 2+ sources
POLA1(5)
0.001 1.000 7.01e-2 7.14e-2 —

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