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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
Huntington disease Salt-sensitive hypertension
1 gene
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1 of 1 corroborated by 2+ sources
ADD1(2)
0.016 0.333 1.18e-2 1.33e-2 ✓ sig. —
Huntington disease Rib fracture
1 gene
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TENM2(1)
0.016 0.500 7.91e-3 9.19e-3 ✓ sig. —
Cerebellar-facial-dental syndrome Huntington disease
1 gene
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1 of 1 corroborated by 2+ sources
BRF1(6)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Congenital brain dysgenesis due to glutamine synthetase deficiency Huntington disease
1 gene
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1 of 1 corroborated by 2+ sources
GLUL(5)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. Cluster 57 →
dilated cardiomyopathy 1V Huntington disease
1 gene
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1 of 1 corroborated by 2+ sources
PSEN2(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Gastroschisis Huntington disease
1 gene
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1 of 1 corroborated by 2+ sources
ADD1(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease hyper-IgE recurrent infection syndrome 5, autosomal recessive
1 gene
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1 of 1 corroborated by 2+ sources
IL6R(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease Interleukin 6 quantitative trait
1 gene
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1 of 1 corroborated by 2+ sources
IL6R(3)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease karyomegalic interstitial nephritis
1 gene
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1 of 1 corroborated by 2+ sources
FAN1(2)
0.016 1.000 3.96e-3 5.02e-3 ✓ sig. —
Huntington disease Pheochromocytoma
3 genes
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3 of 3 corroborated by 2+ sources
MAOA(2), MAOB(2), GDNF(2)
0.040 0.188 3.19e-5 1.48e-4 ✓ sig. —
Hepatic encephalopathy Huntington disease
3 genes
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3 of 3 corroborated by 2+ sources
GLUL(2), MAOA(2), MAOB(2)
0.041 0.214 2.09e-5 9.88e-5 ✓ sig. Cluster 57 →
Dementia in huntington’s disease Huntington disease
2 genes
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2 of 2 corroborated by 2+ sources
PRNP(6), JPH3(6)
0.032 1.000 1.54e-5 7.43e-5 ✓ sig. —
Huntington disease Interstitial nephritis
2 genes
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2 of 2 corroborated by 2+ sources
FAN1(4), MTMR10(2)
0.032 1.000 1.54e-5 7.43e-5 ✓ sig. —
Huntington disease Hypotension
5 genes
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5 of 5 corroborated by 2+ sources
GRIN2B(2), MAOA(2), MAOB(2), IL6(2), CNR1(2)
0.040 0.082 6.60e-6 3.35e-5 ✓ sig. —
Bowen’s disease Huntington disease
3 genes
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3 of 3 corroborated by 2+ sources
NRF1(2), TFAM(2), PPARGC1A(2)
0.048 0.750 2.36e-7 1.55e-6 ✓ sig. —
Huntington disease Mood disorder
12 genes
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5 of 12 corroborated by 2+ sources
GRIK2(1), NRF1(2), BDNF(1), GLUL(1), MAOA(2), MAOB(2), NPY(1), PRNP(6), SIRT1(1), GRIN2A(1), HTT(8), NPY2R(1)
0.034 0.197 1.65e-9 1.47e-8 ✓ sig. —

Showing 16 of 16 matching pairs, sorted by significance (descending). Click a column header to sort.