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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
joubert syndrome 17 Polydactyly
1 gene
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1 of 1 corroborated by 2+ sources
CPLANE1(2)
0.025 1.000 2.53e-3 3.45e-3 ✓ sig. —
joubert syndrome 17 Orofaciodigital syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CPLANE1(7)
0.030 1.000 2.08e-3 2.97e-3 ✓ sig. —
joubert syndrome 17 Uranostaphyloschisis
1 gene
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1 of 1 corroborated by 2+ sources
CPLANE1(2)
0.040 1.000 1.56e-3 2.38e-3 ✓ sig. —
Hydranencephaly joubert syndrome 14
1 gene
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1 of 1 corroborated by 2+ sources
TMEM237(2)
0.043 1.000 1.43e-3 2.23e-3 ✓ sig. Cluster 110 →
Congenital brain malformation joubert syndrome 14
1 gene
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1 of 1 corroborated by 2+ sources
TMEM237(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 110 →
Congenital hypoplasia of part of brain joubert syndrome 14
1 gene
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1 of 1 corroborated by 2+ sources
TMEM237(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 110 →
joubert syndrome 14 Microgyria
1 gene
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1 of 1 corroborated by 2+ sources
TMEM237(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 110 →
Arima syndrome joubert syndrome 14
1 gene
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1 of 1 corroborated by 2+ sources
TMEM237(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
joubert syndrome 1 Penile disease
1 gene
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1 of 1 corroborated by 2+ sources
INPP5E(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
joubert syndrome 17 Monomelic amyotrophy
1 gene
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1 of 1 corroborated by 2+ sources
CPLANE1(2)
0.143 1.000 3.90e-4 8.67e-4 ✓ sig. —
Coach syndrome joubert syndrome 1
1 gene
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1 of 1 corroborated by 2+ sources
INPP5E(2)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. —
Congenital hemivertebra joubert syndrome 1
1 gene
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1 of 1 corroborated by 2+ sources
INPP5E(2)
0.167 1.000 3.25e-4 7.71e-4 ✓ sig. —
Encephalocele joubert syndrome 17
1 gene
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1 of 1 corroborated by 2+ sources
CPLANE1(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 70 →
Congenital hypoplasia of femur joubert syndrome 1
1 gene
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1 of 1 corroborated by 2+ sources
INPP5E(2)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. —
joubert syndrome 1 MORM syndrome
1 gene
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INPP5E(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —

Showing 15 of 15 matching pairs, sorted by significance (descending). Click a column header to sort.