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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
Desbuquois syndrome Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ALX1(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Craniofacial abnormalities Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ALX1(6)
0.006 1.000 1.01e-2 1.15e-2 ✓ sig. —
Frontonasal dysplasia with alopecia and genital anomaly Polydactyly
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(6)
0.025 1.000 2.53e-3 3.45e-3 ✓ sig. —
Christ-siemens-touraine syndrome Craniofrontonasal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
EDA(2)
0.111 0.250 1.30e-3 2.06e-3 ✓ sig. Cluster 117 →
Craniofrontonasal dysplasia Dysphoric mood
1 gene
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1 of 1 corroborated by 2+ sources
EFNB1(7)
0.125 0.250 1.04e-3 1.74e-3 ✓ sig. —
Frontonasal dysplasia Parietal foramina
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(6)
0.111 0.500 9.09e-4 1.58e-3 ✓ sig. —
Craniofrontonasal dysplasia X-linked hypohidrotic ectodermal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
EDA(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 117 →
craniofacial dysplasia - osteopenia syndrome Frontonasal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
IRX5(5)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Frontonasal dysplasia Frontonasal dysplasia with alopecia and genital anomaly
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(7)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Frontonasal dysplasia Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ALX1(7)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Frontonasal dysplasia frontorhiny
1 gene
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1 of 1 corroborated by 2+ sources
ALX3(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Anhidrotic ectodermal dysplasia Craniofrontonasal dysplasia
1 gene
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1 of 1 corroborated by 2+ sources
EDA(2)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 117 →
Craniofrontonasal dysplasia X-linked intellectual disability-cerebellar hypoplasia syndrome
1 gene
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1 of 1 corroborated by 2+ sources
OPHN1(3)
0.200 1.000 2.60e-4 6.51e-4 ✓ sig. Cluster 117 →
11p11.2 deletion syndrome Frontonasal dysplasia with alopecia and genital anomaly
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
Frontonasal dysplasia with alopecia and genital anomaly Potocki-shaffer syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 93 →
Frontonasal dysplasia with alopecia and genital anomaly Parietal foramina
1 gene
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1 of 1 corroborated by 2+ sources
ALX4(8)
0.333 1.000 1.30e-4 3.93e-4 ✓ sig. Cluster 93 →

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