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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
Dementia Prognathism
1 gene
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1 of 1 corroborated by 2+ sources
ADAMTS1(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia pseudohypoaldosteronism type 2D
1 gene
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1 of 1 corroborated by 2+ sources
KLHL3(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
CNGB1-related retinopathy Dementia
1 gene
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1 of 1 corroborated by 2+ sources
CNGB1(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Autoinflammation with episodic fever and immune dysregulation Dementia
1 gene
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1 of 1 corroborated by 2+ sources
SHARPIN(4)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia neuropathy, hereditary sensory and autonomic, type 1A
1 gene
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1 of 1 corroborated by 2+ sources
SPTLC1(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia Intellectual developmental disorder dysmorphic cardiac
1 gene
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1 of 1 corroborated by 2+ sources
TMEM94(4)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia scott syndrome
1 gene
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1 of 1 corroborated by 2+ sources
ANO6(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia Sedoheptulokinase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
SHPK(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. Cluster 2 →
Dementia SMARCC1-associated developmental dysgenesis syndrome
1 gene
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1 of 1 corroborated by 2+ sources
SMARCC1(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia fontaine progeroid syndrome
1 gene
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1 of 1 corroborated by 2+ sources
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia Dihydropteridine reductase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
QDPR(5)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Dementia meier-gorlin syndrome 7
1 gene
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1 of 1 corroborated by 2+ sources
CDC45(2)
0.002 1.000 3.83e-2 4.02e-2 ✓ sig. —
Aicardi syndrome Astrocytoma
1 gene
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1 of 1 corroborated by 2+ sources
TEAD1(2)
0.003 0.500 3.87e-2 4.06e-2 ✓ sig. —
Ankle fracture Uterine fibroid
1 gene
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CPED1(1)
0.003 0.500 3.94e-2 4.12e-2 ✓ sig. —
3-hydroxyisobutyryl-coa hydrolase deficiency Glioblastoma
1 gene
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1 of 1 corroborated by 2+ sources
HIBCH(3)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma ornithine aminotransferase deficiency
1 gene
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1 of 1 corroborated by 2+ sources
OAT(2)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Cataract-microcornea-metabolic syndrome Glioblastoma
1 gene
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1 of 1 corroborated by 2+ sources
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies
1 gene
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1 of 1 corroborated by 2+ sources
RAP1B(2)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. Cluster 284 →
Glioblastoma leukodystrophy, hypomyelinating, 14
1 gene
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1 of 1 corroborated by 2+ sources
UFM1(2)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma Microscopic polyangiitis
1 gene
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CDH19(1)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Giant cell tumor of bone Glioblastoma
1 gene
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H3-3A(1)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma Rin2 syndrome
1 gene
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1 of 1 corroborated by 2+ sources
RIN2(5)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma Sarcosinemia
1 gene
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1 of 1 corroborated by 2+ sources
SARDH(7)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. —
Glioblastoma systemic lupus erythematosus 18
1 gene
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1 of 1 corroborated by 2+ sources
PLD4(2)
0.002 1.000 3.94e-2 4.13e-2 ✓ sig. Cluster 284 →
neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties Ulcerative colitis
1 gene
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1 of 1 corroborated by 2+ sources
DPH5(2)
0.002 1.000 3.97e-2 4.15e-2 ✓ sig. Cluster 28 →

Showing 25 of 20813 pairs, sorted by significance (ascending). Click a column header to sort.