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
Larsen syndrome spondyloepiphyseal dysplasia with congenital joint dislocations
1 gene
Show details
1 of 1 corroborated by 2+ sources
CHST3(4)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Cutaneous mastocytosis Telangiectasia macularis eruptiva perstans
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIT(3)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Atrioventricular block dilated cardiomyopathy 1HH
1 gene
Show details
1 of 1 corroborated by 2+ sources
BAG3(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 4 →
Atrioventricular block dilated cardiomyopathy 1I
1 gene
Show details
1 of 1 corroborated by 2+ sources
DES(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 4 →
Donohue syndrome Toxic nodular goiter
1 gene
Show details
1 of 1 corroborated by 2+ sources
INSR(7)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Congenital neutropenia Dursun syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
G6PC3(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
dysosteosclerosis Osteopetrosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCIRG1(8)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Congenital neutropenia dysosteosclerosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCIRG1(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
ectodermal dysplasia and immunodeficiency 2 Hodgkin disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
NFKBIA(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
EEM syndrome Hypotrichosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDH3(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Cutaneous mastocytosis EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition
1 gene
Show details
1 of 1 corroborated by 2+ sources
EGLN1(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
ehlers-danlos syndrome, spondylodysplastic type, 1 Larsen syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
B4GALT7(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 68 →
Chondrodysplasia Eiken skeletal dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTH1R(6)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Congenital myelofibrosis with anemia Congenital neutropenia
1 gene
Show details
1 of 1 corroborated by 2+ sources
RBSN(3)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 209 →
Congenital neutropenia Neutrophilic leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
CSF3R(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 209 →
Congenital neutropenia Neutropenia, nonimmune chronic idiopathic, adult
1 gene
Show details
1 of 1 corroborated by 2+ sources
GFI1(3)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 209 →
Craniofacial anomalies with anterior segment dysgenesis Eye abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
VSX1(5)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Cutaneous mastocytosis Hemoglobinopathy toms river
1 gene
Show details
1 of 1 corroborated by 2+ sources
HBG2(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Congenital neutropenia Cyclic hematopoiesis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ELANE(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Deafness with congenital heart defects and posterior embryotoxon Eye abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
JAG1(4)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Dentin dysplasia Tricho-dento-osseous syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DLX3(6)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Dentin dysplasia Enamel-renal syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAM20A(2)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 366 →
Coffin-siris syndrome familial meningioma
1 gene
Show details
1 of 1 corroborated by 2+ sources
SMARCE1(7)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
FLNB-associated autosomal dominant filamin related bone disorder Larsen syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FLNB(7)
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. —
Eye abnormalities frank-ter haar syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.056 1.000 1.10e-3 1.83e-3 ✓ sig. Cluster 14 →

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