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
Sensory peripheral neuropathy Wilson disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP7B(5)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Severe neonatal spondylometaphyseal dysplasia Shwachman-diamond syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SBDS(7)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 159 →
Mucolipidosis Sialidosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
NEU1(5)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Russell-silver syndrome silver-russell syndrome 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
IGF2(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Generalized lipodystrophy spondylometaphyseal dysplasia-cone-rod dystrophy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PCYT1A(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 71 →
Developmental delay with autism spectrum disorder Skin hair eye pigmentation variation
1 gene
Show details
1 of 1 corroborated by 2+ sources
HERC2(4)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Diabetes mellitus ketosis prone Ventricular outflow obstruction
1 gene
Show details
1 of 1 corroborated by 2+ sources
INS(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency Diabetes mellitus ketosis prone
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTLA4(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
dilated cardiomyopathy 1C Distal muscular dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
LDB3(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Disabling pansclerotic morphea of childhood Uveomeningoencephalitic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
STAT4(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 1 →
Distal axonal motor neuropathy-myofibrillar myopathy syndrome Distal muscular dystrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
HSPB8(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Distal muscular dystrophy Hereditary axonal motor and sensory neuropathy
1 gene
Show details
BICD2(1)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Distal muscular dystrophy distal myopathy with vocal cord weakness
1 gene
Show details
1 of 1 corroborated by 2+ sources
MATR3(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
distal myopathy with vocal cord weakness Vogt-koyanagi-harada disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
MATR3(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 1 →
46,xy sex reversal Dosage-sensitive sex reversal
1 gene
Show details
1 of 1 corroborated by 2+ sources
NR0B1(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
DPAGT1-congenital disorder of glycosylation Tubular aggregate myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
DPAGT1(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 217 →
Cerebellar diseases dyskeratosis congenita, autosomal dominant 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
TINF2(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 130 →
Benign hereditary chorea Dyskinesia with orofacial involvement
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADCY5(6)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Benign hereditary chorea Dyskinesia, familial, with facial myokymia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADCY5(3)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Dysthymic disorder Early-onset obesity-hyperphagia-severe developmental delay syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NTRK2(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 156 →
Dacryocystitis Dysthymic disorder
1 gene
Show details
IL1RN(1)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Dysthymic disorder Sclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL1RN(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —
Dystrophinopathy Leiomyosarcoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
DMD(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 213 →
Early-onset epilepsy-intellectual disability-brain anomalies syndrome Wolf-hirschhorn syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIGG(2)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. Cluster 159 →
East syndrome Pendred syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KCNJ10(7)
0.125 1.000 4.55e-4 9.73e-4 ✓ sig. —

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