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
Congenital isolated acth deficiency Pituitary stalk interruption syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TBX19(4)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Congenital membranous nephropathy Membranous glomerulonephritis
1 gene
Show details
1 of 1 corroborated by 2+ sources
MME(3)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Congenital microcephaly congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ASNS(5)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Biliary atresia Tetrahydrobiopterin-responsive phenylketonuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
PAH(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Neuronal ceroid lipofuscinosis Visceral acid sphingomyelinase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMPD1(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Seborrheic keratosis Woolly hair-skin fragility syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TUFT1(4)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. Cluster 29 →
Hyperplasia palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KDM1A(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Hyperplasia Peters plus syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
B3GLCT(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. Cluster 143 →
Pancreatic ductal carcinoma peutz-jeghers syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
STK11(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Biliary atresia Phenylketonuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
PAH(4)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Pituitary stalk interruption syndrome PMM2-congenital disorder of glycosylation
1 gene
Show details
1 of 1 corroborated by 2+ sources
PMM2(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Auditory neuropathy progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIAPH1(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Congenital ear anomaly hearing impairment and infertile male syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDC14A(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Congenital ear anomaly Hearing loss with hypertrophic cardiomyopathy
1 gene
Show details
MYO6(1)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Distal spinal muscular atrophy hereditary peripheral neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
IGHMBP2(4)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Distal spinal muscular atrophy hereditary sensory and autonomic neuropathy type 6
1 gene
Show details
1 of 1 corroborated by 2+ sources
DST(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Homocystinuria Neural tube defects, x-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
CBS(4)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
hypercholesterolemia, familial, 1 Hyperplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
LDLR(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
hyperinsulinemic hypoglycemia with polycystic kidney disease Pituitary stalk interruption syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PMM2(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
hypogonadotropic hypogonadism 3 with or without anosmia Pituitary stalk interruption syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PROKR2(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Congenital posterior urethral valves Seborrheic keratosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
BNC2(2)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. Cluster 29 →
Biliary atresia Congenitally uncorrected transposition of the great arteries
1 gene
Show details
CFC1(1)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. —
Auditory neuropathy Deafness dystonia syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TIMM8A(3)
0.031 1.000 2.01e-3 2.90e-3 ✓ sig. Cluster 26 →
Cushing syndrome Ocular hypertension
2 genes
Show details
2 of 2 corroborated by 2+ sources
NR3C1(3), CDH23(2)
0.029 0.095 2.00e-3 2.90e-3 ✓ sig. —
Aplastic anemia Esophageal atresia
2 genes
Show details
1 of 2 corroborated by 2+ sources
TERT(5), GSTM1(1)
0.032 0.063 2.00e-3 2.90e-3 ✓ sig. —

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