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
Deafness and myopia high myopia-sensorineural deafness syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLITRK6(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Deafness with congenital and adult-onset progressive leukodystrophy Early onset progressive leukoencephalopathy-central nervous system calcification-hearing loss-visual impairment syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KARS1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Deafness with congenital and adult-onset progressive leukodystrophy Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KARS1(4)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Deafness with congenital heart defects and posterior embryotoxon Hepatic ductular hypoplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
JAG1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 356 →
Deafness with labyrinthine aplasia, microtia, and microdontia Otodental dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGF3(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Deafness-lymphedema-leukemia syndrome Gata2 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA2(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 136 →
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome Focal epilepsy-intellectual disability-cerebro-cerebellar malformation
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBC1D24(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 90 →
Delta zero thalassemia Delta-thalassemia
1 gene
Show details
HBD(1)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Delta zero thalassemia Hemoglobin lepore beta thalassemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HBD(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Delta-sarcoglycan-related limb-girdle muscular dystrophy r6 dilated cardiomyopathy 1L
1 gene
Show details
1 of 1 corroborated by 2+ sources
SGCD(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Delta-thalassemia Hemoglobin lepore beta thalassemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HBD(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Demyelinating leukodystrophy microcephaly 26, primary, autosomal dominant
1 gene
Show details
1 of 1 corroborated by 2+ sources
LMNB1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Den hoed-de boer-voisin syndrome Developmental delay with dysmorphic facies and dental anomalies
1 gene
Show details
1 of 1 corroborated by 2+ sources
SATB1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Denys drash syndrome Drash syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
WT1(7)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 35 →
Denys drash syndrome wilms tumor 1
1 gene
Show details
1 of 1 corroborated by 2+ sources
WT1(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 35 →
Dermatofibrosis lenticularis disseminata Osteopoikilosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEMD3(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 175 →
Dermatopathia pigmentosa reticularis Epidermolysis bullosa simplex
1 gene
Show details
1 of 1 corroborated by 2+ sources
KRT14(6)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 269 →
developmental and epileptic encephalopathy, 29 Leukoencephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
AARS1(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental delay and seizures DHDDS-CDG
1 gene
Show details
1 of 1 corroborated by 2+ sources
DHDDS(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental delay due to metabolic enzyme deficiency methylmalonate semialdehyde dehydrogenase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ALDH6A1(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental delay with ataxia, hypotonia, and facial dysmorphism hypotonia, ataxia, and delayed development syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EBF3(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 323 →
Developmental delay with hypotonia and behavioral abnormalities floating-harbor syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SRCAP(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental delay with immunodeficiency syndrome immunodeficiency, developmental delay, and hypohomocysteinemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFE2L2(3)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental delay with intellectual disability and obesity PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PHIP(2)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. —
Developmental malformations-deafness-dystonia syndrome Dystonia-deafness syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ACTB(5)
0.500 1.000 6.49e-5 2.33e-4 ✓ sig. Cluster 186 →

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