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
Encephalopathy due to mitochondrial and peroxisomal fission defect Exostoses
1 gene
Show details
1 of 1 corroborated by 2+ sources
MFF(2)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Idiopathic steroid-resistant nephrotic syndrome Nephrotic syndrome, steroid-resistant, autosomal recessive
1 gene
Show details
1 of 1 corroborated by 2+ sources
NPHS2(2)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Multinodular goiter Ochoa syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HPSE2(2)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Intellectual developmental disorder dysmorphic cerebellar Leber hereditary optic neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CYTB(2)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Hypertriglyceridemia Interstitial nephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAN1(4)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Intestinal hypomagnesemia Mastocytosis
1 gene
Show details
TRPV6(1)
0.033 0.500 3.63e-3 4.67e-3 ✓ sig. —
Delirium, dementia, and cognitive disorders Intracranial hypertension
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC4A10(2)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Clonal hematopoiesis Isolated anhidrosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITPR2(3)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Atrophic macular degeneration Cerebellar vermis atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SYN3(2)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Chops syndrome Delirium, dementia, and cognitive disorders
1 gene
Show details
1 of 1 corroborated by 2+ sources
AFF4(3)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome Delirium, dementia, and cognitive disorders
1 gene
Show details
1 of 1 corroborated by 2+ sources
AFF4(4)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Clonal hematopoiesis skeletal dysplasia, mild, with joint laxity and advanced bone age
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Bell's palsy spermatogenic failure 46
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAH8(2)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Atrophic macular degeneration BARD1-related cancer predisposition
1 gene
Show details
1 of 1 corroborated by 2+ sources
BARD1(2)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Delirium, dementia, and cognitive disorders ornithine carbamoyltransferase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
OTC(2)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Apolipoprotein c-iii deficiency Delirium, dementia, and cognitive disorders
1 gene
Show details
1 of 1 corroborated by 2+ sources
APOC3(4)
0.018 1.000 3.64e-3 4.67e-3 ✓ sig. —
Blepharoptosis Marinesco-sjogren syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SIL1(6)
0.045 0.333 3.70e-3 4.74e-3 ✓ sig. —
neurometabolic disorder due to serine deficiency Neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
PHGDH(2)
0.045 0.333 3.70e-3 4.74e-3 ✓ sig. —
nephrotic syndrome, type 20 Pancreatitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBC1D8B(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —
Movement disorder Neurodegeneration peripheral neuropathy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN6(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —
Movement disorder neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN6(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —
Neutropenia Neutrophilic leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSF3R(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. Cluster 209 →
Ablepharon macrostomia syndrome Dry eye syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TWIST2(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —
Focal glomerulosclerosis schimke immuno-osseous dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —
Movement disorder spinocerebellar ataxia type 29
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITPR1(2)
0.017 1.000 3.70e-3 4.74e-3 ✓ sig. —

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