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
Hypo-akinesia disorder of prenatal onset Myasthenia gravis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHRNG(4)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
hypogonadotropic hypogonadism 4 with or without anosmia Kallmann syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PROK2(5)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. Cluster 54 →
hypotonia, ataxia, and delayed development syndrome Vesicoureteral reflux
1 gene
Show details
1 of 1 corroborated by 2+ sources
EBF3(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. Cluster 323 →
Dermatitis Ichthyosis vulgaris
1 gene
Show details
1 of 1 corroborated by 2+ sources
FLG(3)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Familial cylindromatosis Uterine neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYLD(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Dermatitis familial meningioma
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMARCE1(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Developmental delay floating-harbor syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SRCAP(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Focal dermal hypoplasia Microphthalmia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PORCN(8)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. Cluster 56 →
Dermatitis Focal palmoplantar keratoderma with joint keratoses
1 gene
Show details
1 of 1 corroborated by 2+ sources
DSG1(3)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
frontotemporal dementia and/or amyotrophic lateral sclerosis 8 Uterine neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYLD(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Cone dystrophy GNAT2-related retinopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNAT2(4)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
15q11q13 microduplication syndrome Developmental delay
1 gene
Show details
1 of 1 corroborated by 2+ sources
UBE3A(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
2-aminoadipic 2-oxoadipic aciduria Dejerine-sottas disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
DHTKD1(6)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
2-aminoadipic 2-oxoadipic aciduria Hypertrophic neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
DHTKD1(6)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
2-aminoadipic 2-oxoadipic aciduria Roussy-levy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DHTKD1(6)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Arboleda-tham syndrome Developmental delay
1 gene
Show details
1 of 1 corroborated by 2+ sources
KAT6A(3)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Dermatitis renal hypomagnesemia 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
EGF(3)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Cone dystrophy retinitis pigmentosa 47
1 gene
Show details
1 of 1 corroborated by 2+ sources
SAG(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Cone dystrophy retinitis pigmentosa 65
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDHR1(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. Cluster 7 →
Limb girdle muscular dystrophy Sarcotubular myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIM32(6)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Left ventricular noncompaction cardiomyopathy Sensorineural deafness with dilated cardiomyopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
EYA4(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Cholangiocarcinoma Serrated polyposis
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNF43(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Cholangiocarcinoma sessile serrated polyposis cancer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNF43(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Dermatitis severe combined immunodeficiency due to IKK2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
IKBKB(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. —
Left ventricular noncompaction cardiomyopathy sick sinus syndrome 2, autosomal dominant
1 gene
Show details
1 of 1 corroborated by 2+ sources
HCN4(2)
0.026 1.000 2.47e-3 3.37e-3 ✓ sig. Cluster 4 →

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