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
Renal cell carcinoma X-linked syndromic complex neurodevelopmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TFE3(2)
0.007 0.333 2.68e-2 2.86e-2 ✓ sig. —
Androgenetic alopecia Weiss-kruszka syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZNF462(5)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Intellectual developmental disorder growth metabolic
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIP2B(3)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia isovaleric acidemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
IVD(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia hao-fountain syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
USP7(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia hypomyelinating leukodystrophy 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
AIMP1(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Catifa syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RIC1(5)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia exostoses, multiple, type 2
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXT2(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Combined oxidative phosphorylation defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
WARS2(3)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Perlman syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIS3L2(5)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
16p13.2 microdeletion syndrome Androgenetic alopecia
1 gene
Show details
1 of 1 corroborated by 2+ sources
USP7(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Absence of fingerprints-congenital milia syndrome Androgenetic alopecia
1 gene
Show details
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
amyotrophic lateral sclerosis type 15 Androgenetic alopecia
1 gene
Show details
1 of 1 corroborated by 2+ sources
UBQLN2(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive
1 gene
Show details
1 of 1 corroborated by 2+ sources
EDAR(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Retrograde amnesia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PREP(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Rhizomelic limb shortening with dysmorphic features
1 gene
Show details
1 of 1 corroborated by 2+ sources
PKDCC(5)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia scalp-ear-nipple syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCTD1(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia Seizures, scoliosis, and macrocephaly/microcephaly syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXT2(5)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATAD2B(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia syndromic multisystem autoimmune disease due to ITCH deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITCH(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Androgenetic alopecia bamforth-lazarus syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FOXE1(2)
0.002 1.000 2.65e-2 2.83e-2 ✓ sig. —
Intellectual developmental disorder neuropsychiatric Migraine
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC45A1(4)
0.002 1.000 2.62e-2 2.80e-2 ✓ sig. —
Migraine neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLR2A(2)
0.002 1.000 2.62e-2 2.80e-2 ✓ sig. —
Migraine Trichilemmal cyst
1 gene
Show details
1 of 1 corroborated by 2+ sources
BPIFC(3)
0.002 1.000 2.62e-2 2.80e-2 ✓ sig. Cluster 78 →
Migraine Weiss-kruszka syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZNF462(5)
0.002 1.000 2.62e-2 2.80e-2 ✓ sig. —

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