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
Cloves syndrome Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIK3CA(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Congenital microvillous atrophy Microvillus inclusion disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
MYO5B(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Myoclonus-renal failure syndrome Unverricht-lundborg syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SCARB2(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 329 →
Hyperkalemic periodic paralysis Myotonia congenita
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN1(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neonatal convulsions Sensorineural hearing loss thrombocytopenia syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIAPH1(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neonatal convulsions progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DIAPH1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neonatal convulsions Schilder disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
POLG(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 97 →
Neovascular inflammatory vitreoretinopathy Vitreoretinopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CAPN5(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 11 →
Nephropathic cystinosis Ocular cystinosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTNS(5)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neurofibrosarcoma Schimmelpenning-feuerstein-mims syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
NRAS(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 18 →
neurometabolic disorder due to serine deficiency Phosphoserine phosphatase deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
PSPH(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neuropathic spinal arthropathy Rupture, spontaneous
1 gene
Show details
1 of 1 corroborated by 2+ sources
COL5A1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Neuropathic spinal arthropathy Simpson syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
KAT6B(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Mandibuloacral dysostosis obsolete lethal restrictive dermopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 65 →
obsolete PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis Xerocytosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIEZO1(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Oropharyngeal dysphagia Spinocerebellar ataxia, x-linked
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATP2B3(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Osteoglophonic dysplasia Pfeiffer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR1(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Osteoglophonic dysplasia Trigonocephaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR1(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 185 →
Osteolysis, hereditary multicentric Torg-winchester syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
MMP2(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Osteoma cutis Primary bilateral macronodular adrenal hyperplasia
1 gene
Show details
1 of 1 corroborated by 2+ sources
GNAS(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 409 →
Growth retardation, mild developmental delay, chronic hepatitis syndrome Polycythemia, primary familial and congenital
1 gene
Show details
1 of 1 corroborated by 2+ sources
SH2B3(3)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Hairy cell leukemia Ventricular hypertrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
BRAF(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
hartnup disease Hyperglycinuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC6A19(2)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Hartsfield-Bixler-Demyer syndrome Pfeiffer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR1(7)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. —
Hartsfield-Bixler-Demyer syndrome Trigonocephaly
1 gene
Show details
1 of 1 corroborated by 2+ sources
FGFR1(4)
0.250 1.000 1.95e-4 5.35e-4 ✓ sig. Cluster 185 →

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