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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.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Intellectual developmental disorder X-linked intellectual disability, Cabezas type
1 gene
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1 of 1 corroborated by 2+ sources
CUL4B(2)
0.001 1.000 5.25e-2 5.42e-2 —
Intellectual developmental disorder Urocanate hydratase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
UROC1(7)
0.001 1.000 5.25e-2 5.42e-2 —
Developmental delay with behavioral abnormalities Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
ADGRL1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Developmental delay with overweight and facial dysmorphism Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
SRRM2(5)
0.001 1.000 5.25e-2 5.42e-2 —
Diffuse cerebral and cerebellar atrophy–intractable seizures–progressive microcephaly syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
QARS1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Early-onset epilepsy-intellectual disability-brain anomalies syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
PIGG(4)
0.001 1.000 5.25e-2 5.42e-2 —
Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
OTUD6B(2)
0.001 1.000 5.25e-2 5.42e-2 —
Ectopic thyroid tissue Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
FBXO31(5)
0.001 1.000 5.25e-2 5.42e-2 —
El-hayek-chahrour neurodevelopmental syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
KDM5A(5)
0.001 1.000 5.25e-2 5.42e-2 —
Hemiparkinsonism hemiatrophy syndrome Intellectual developmental disorder
1 gene
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H3-3B(1)
0.001 1.000 5.25e-2 5.42e-2 —
hereditary spastic paraplegia 18 Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
ERLIN2(3)
0.001 1.000 5.25e-2 5.42e-2 —
holoprosencephaly 12 with or without pancreatic agenesis Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
CNOT1(2)
0.001 1.000 5.25e-2 5.42e-2 —
hypomyelinating leukodystrophy 5 Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
HYCC1(3)
0.001 1.000 5.25e-2 5.42e-2 —
hypotonia, infantile, with psychomotor retardation and characteristic facies 2 Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
UNC80(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Alpha-mannosidosis Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
MAN2B1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Allan-herndon-dudley syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
SLC16A2(3)
0.001 1.000 5.25e-2 5.42e-2 —
ALG3-congenital disorder of glycosylation Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
ALG3(2)
0.001 1.000 5.25e-2 5.42e-2 —
Acromelic frontonasal dysostosis Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
ZSWIM6(2)
0.001 1.000 5.25e-2 5.42e-2 —
aspartylglucosaminuria Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
AGA(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Autism-epilepsy syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
BCKDK(2)
0.001 1.000 5.25e-2 5.42e-2 —
autosomal recessive spinocerebellar ataxia 14 Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
SPTBN2(2)
0.001 1.000 5.25e-2 5.42e-2 —
autosomal recessive spinocerebellar ataxia 20 Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
SNX14(3)
0.001 1.000 5.25e-2 5.42e-2 —
Bafopathy Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
ACTL6A(3)
0.001 1.000 5.25e-2 5.42e-2 —
basilicata-akhtar syndrome Intellectual developmental disorder
1 gene
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1 of 1 corroborated by 2+ sources
MSL3(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Intellectual developmental disorder NAA10-related syndrome
1 gene
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1 of 1 corroborated by 2+ sources
NAA10(2)
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.