Log in to save this analysis

Save This Analysis

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.
0 selected Clear
Disease A ⇵Disease B ⇵Shared genes ⇵Similarity score ⇵Overlap coefficient ⇵P-value ⇵FDR q-value ▼ Shared cluster
Congenital scoliosis Weill-marchesani syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBN1(7)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 52 →
Cardiac injury Wernicke-korsakoff syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALDH2(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Polycystic kidney disease with tuberous sclerosis Xanthinuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
TSC2(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 70 →
Polycystic kidneys, severe infantile with tuberous sclerosis Xanthinuria
1 gene
Show details
TSC2(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 70 →
Deafness, digenic Xeroderma
1 gene
Show details
1 of 1 corroborated by 2+ sources
GJB2(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 322 →
Senter syndrome Xeroderma
1 gene
Show details
GJB2(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Colorectal cancer susceptibility non-severe combined immunodeficiency due to polymerase delta deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLD1(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 410 →
Colorectal cancer susceptibility Xfe progeroid syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLE(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Anaplastic astrocytoma Combined d-2- and l-2-hydroxyglutaric aciduria
1 gene
Show details
1 of 1 corroborated by 2+ sources
IDH2(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Anaplastic oligodendroglioma Combined d-2- and l-2-hydroxyglutaric aciduria
1 gene
Show details
1 of 1 corroborated by 2+ sources
IDH2(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia Neural tube defects, folate-sensitive
1 gene
Show details
1 of 1 corroborated by 2+ sources
MTHFD1(5)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
complex neurodevelopmental disorder with or without congenital anomalies Developmental delay with or without intellectual or behavioral abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRRAP(5)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Anisometropia Concussion
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTEN(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 291 →
Concussion Lipomatosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTEN(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 291 →
Congenital keratoglobus Primary congenital glaucoma
1 gene
Show details
LTBP2(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Congenital keratoglobus Weill-marchesani syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
LTBP2(6)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Congenital mirror movements Horizontal gaze palsy with progressive scoliosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
DCC(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Coronary vasospasm Renovascular hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
NOS3(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Cortical dysplasia Cortical occipital malformations
1 gene
Show details
TBR1(1)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 275 →
Cortical dysplasia Developmental delay with language impairment and movement disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBR1(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 275 →
Cortical dysplasia Intellectual developmental disorder autism speech
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBR1(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 275 →
Craniofrontonasal dysplasia X-linked hypohidrotic ectodermal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
EDA(3)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. Cluster 117 →
Cri-du-chat syndrome Macrocytic anemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TERT(2)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Anaplastic astrocytoma D-2-hydroxyglutaric aciduria
1 gene
Show details
1 of 1 corroborated by 2+ sources
IDH2(5)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —
Anaplastic oligodendroglioma D-2-hydroxyglutaric aciduria
1 gene
Show details
1 of 1 corroborated by 2+ sources
IDH2(5)
0.167 0.500 5.19e-4 1.06e-3 ✓ sig. —

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