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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
Lymphatic malformation Non-immune hydrops fetalis
6 genes
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6 of 6 corroborated by 2+ sources
EPHB4(4), PIEZO1(5), THSD1(4), ANGPT2(4), CALCRL(4), FLT4(5)
0.113 0.462 7.44e-13 9.12e-12 ✓ sig. —
congenital heart defects, multiple types, 7 lymphatic malformation 1
1 gene
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FLT4(1)
0.500 1.000 6.49e-5 2.32e-4 ✓ sig. —
Hydrops fetalis Lymphatic malformation
2 genes
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2 of 2 corroborated by 2+ sources
CELSR1(4), PIEZO1(5)
0.071 0.154 7.84e-5 2.79e-4 ✓ sig. —
Capillary infantile hemangioma lymphatic malformation 1
1 gene
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1 of 1 corroborated by 2+ sources
FLT4(3)
0.250 1.000 1.95e-4 5.32e-4 ✓ sig. —
Lymphatic malformation Primary microcephaly
2 genes
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2 of 2 corroborated by 2+ sources
MCPH1(3), ANGPT2(4)
0.043 0.154 3.85e-4 8.64e-4 ✓ sig. —
congenital heart defects, multiple types, 7 Lymphatic malformation
1 gene
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1 of 1 corroborated by 2+ sources
FLT4(4)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
Congenital primary lymphedema of gordon Lymphatic malformation
1 gene
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1 of 1 corroborated by 2+ sources
VEGFC(6)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
EPHB4-associated vascular malformation spectrum Lymphatic malformation
1 gene
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1 of 1 corroborated by 2+ sources
EPHB4(5)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
hypomyelinating leukodystrophy 2 Lymphatic malformation
1 gene
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1 of 1 corroborated by 2+ sources
GJC2(6)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
Lymphatic malformation Yellow nail syndrome
1 gene
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1 of 1 corroborated by 2+ sources
CELSR1(5)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
Lymphatic malformation lymphatic malformation 1
1 gene
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1 of 1 corroborated by 2+ sources
FLT4(4)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
Lymphatic malformation microcephaly with intellectual disability
1 gene
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1 of 1 corroborated by 2+ sources
MCPH1(2)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
Lymphatic malformation obsolete PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis
1 gene
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1 of 1 corroborated by 2+ sources
PIEZO1(5)
0.071 1.000 8.44e-4 1.50e-3 ✓ sig. —
lymphatic malformation 1 Lymphedema
1 gene
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1 of 1 corroborated by 2+ sources
FLT4(3)
0.059 1.000 1.04e-3 1.74e-3 ✓ sig. —
lymphatic malformation 1 Non-immune hydrops fetalis
1 gene
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1 of 1 corroborated by 2+ sources
FLT4(2)
0.022 1.000 2.92e-3 3.88e-3 ✓ sig. —
Breast neoplasms Diffuse lymphatic malformation
1 gene
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1 of 1 corroborated by 2+ sources
ARAF(2)
0.002 1.000 3.36e-2 3.56e-2 ✓ sig. Cluster 4 →

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