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
geroderma osteodysplastica Skin abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
GORAB(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 377 →
Gilbert syndrome Serum bilirubin level
1 gene
Show details
1 of 1 corroborated by 2+ sources
UGT1A1(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Growth hormone deficiency with pituitary anomalies Septo-optic dysplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
HESX1(5)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 218 →
Ectrodactyly Sebaceous gland neoplasms
1 gene
Show details
1 of 1 corroborated by 2+ sources
LEF1(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Omenn syndrome severe combined immunodeficiency due to DCLRE1C deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
DCLRE1C(5)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 173 →
Omenn syndrome severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADA(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Headache short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC10A7(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 126 →
Saldino-noonan syndrome short-rib thoracic dysplasia 11 with or without polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYNC2I2(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 22 →
Craniodiaphyseal dysplasia short-rib thoracic dysplasia 16 with or without polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
IFT52(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 22 →
Saldino-noonan syndrome short-rib thoracic dysplasia 17 with or without polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYNLT2B(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 22 →
Craniodiaphyseal dysplasia short-rib thoracic dysplasia 7 with or without polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
WDR35(6)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 22 →
Saldino-noonan syndrome short-rib thoracic dysplasia 8 with or without polydactyly
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYNC2I1(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 22 →
Beckwith-wiedemann syndrome silver-russell syndrome 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
IGF2(6)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Acro-dermo-ungual-lacrimal-tooth syndrome Skin abnormalities
1 gene
Show details
1 of 1 corroborated by 2+ sources
TP63(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Delirium SLC6A3-related dopamine transporter deficiency syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC6A3(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Septo-optic dysplasia SOX3-related X-linked pituitary hormone deficiency with or without intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOX3(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Epiphyseal dysplasia Stickler syndrome, type 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL9A1(6)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 248 →
Brachycephaly Sweeney-cox syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TWIST1(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 127 →
Omenn syndrome T-B+ severe combined immunodeficiency due to gamma chain deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
IL2RG(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Goldenhar syndrome T-cell immunodeficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
FOXI3(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 48 →
Dwarfism Tatton-Brown-Rahman overgrowth syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNMT3A(3)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Brachycephaly TCF12-related craniosynostosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCF12(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. Cluster 127 →
15q11q13 microduplication syndrome Angelman syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
UBE3A(7)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
16q24.3 microdeletion syndrome Esotropia
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANKRD11(2)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —
Acatalasia Keratosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CAT(4)
0.091 1.000 6.49e-4 1.24e-3 ✓ sig. —

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