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
optic atrophy 9 Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACO2(2)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
lymphoproliferative syndrome 1 Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITK(2)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Catifa syndrome Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
RIC1(5)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
ITPKB deficiency Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITPKB(2)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Autoinflammation with episodic fever and immune dysregulation Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
SHARPIN(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Axonal neuropathy with neuromyotonia Respiratory system disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
HINT1(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Male infertility globozoospermia Teratozoospermia
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPATA16(2)
0.028 0.111 1.57e-2 1.73e-2 ✓ sig. —
Mitochondrial disease Mitochondrial encephalocardiomyopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TMEM70(3)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. Cluster 50 →
Mitochondrial disease optic atrophy 11
1 gene
Show details
1 of 1 corroborated by 2+ sources
YME1L1(3)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Mitochondrial disease optic atrophy 9
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACO2(3)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Deafness, encephaloneuropathy, obesity, valvulopathy syndrome Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
PDSS1(5)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Mitochondrial disease Spastic ataxia optic atrophy dysarthria syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MTPAP(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Mitochondrial disease Spastic ataxia with leukoencephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
MARS2(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Combined oxidative phosphorylation defect Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
WARS2(3)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
hyperphosphatasia with intellectual disability syndrome 6 Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIGY(2)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Early-onset dystonia with spastic paraplegia Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP5MC3(5)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. Cluster 50 →
autosomal recessive optic atrophy, OPA7 type Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
3-hydroxyisobutyryl-coa hydrolase deficiency Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
HIBCH(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Aminoglycoside-induced deafness Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRMU(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Mitochondrial disease Pancreatic insufficiency syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COX4I2(6)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. Cluster 50 →
Mitochondrial disease Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRMT5(5)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. Cluster 50 →
Childhood-onset dystonia Mitochondrial disease
1 gene
Show details
MECR(1)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
MECR(4)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Mitochondrial disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHCHD10(3)
0.004 1.000 1.57e-2 1.73e-2 ✓ sig. —
Central vertigo Ocular hypertension
1 gene
Show details
OTOGL(1)
0.019 0.200 1.58e-2 1.74e-2 ✓ sig. —

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