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
Dental caries Dyggve-melchior-clausen syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DYM(6)
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Dental caries microcornea-myopic chorioretinal atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Dental caries ITPKB deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITPKB(2)
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Dental caries phosphohydroxylysinuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
PHYKPL(2)
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Dental caries X-linked immune dysregulation with inflammatory bowel disease due to elf4 deficiency
1 gene
Show details
1 of 1 corroborated by 2+ sources
ELF4(2)
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Dental caries fontaine progeroid syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.004 1.000 1.50e-2 1.66e-2 ✓ sig. —
Sclerosing cholangitis Thauvin-robinet-faivre syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FIBP(3)
0.004 1.000 1.49e-2 1.66e-2 ✓ sig. —
Sclerosing cholangitis Xy gonadal dysgenesis syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PPP2R3C(2)
0.004 1.000 1.49e-2 1.66e-2 ✓ sig. —
Partial corpus callosum agenesis Sclerosing cholangitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
KPNA7(3)
0.004 1.000 1.49e-2 1.66e-2 ✓ sig. —
Hyaline fibromatosis Sclerosing cholangitis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANTXR2(3)
0.004 1.000 1.49e-2 1.66e-2 ✓ sig. —
Keratinocyte carcinoma Uncombable hair syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TGM3(6)
0.013 0.333 1.49e-2 1.65e-2 ✓ sig. —
Lymphocytic leukemia Thiamine metabolism dysfunction syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TPK1(4)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Ovarian epithelial cancer Sarcoglycanopathies
1 gene
Show details
1 of 1 corroborated by 2+ sources
SGCG(2)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Childhood kidney wilms tumor Ovarian epithelial cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTR9(2)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Developmental delay with variable intellectual disability Lymphocytic leukemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
JARID2(5)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Myoadenylate deaminase deficiency Ovarian epithelial cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
AMPD1(2)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Congenital neurologic anomalies Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRMT10A(3)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Congenital neurologic anomalies Intellectual developmental disorder seizures speech
1 gene
Show details
NTNG2(1)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Congenital neurologic anomalies Lafora disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPM2A(4)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Lafora disease Ovarian epithelial cancer
1 gene
Show details
1 of 1 corroborated by 2+ sources
EPM2A(5)
0.009 0.500 1.49e-2 1.65e-2 ✓ sig. —
Bronchopneumonia Urticaria
1 gene
Show details
CBLB(1)
0.020 0.200 1.48e-2 1.65e-2 ✓ sig. —
Canavan disease Premature ovarian failure
1 gene
Show details
1 of 1 corroborated by 2+ sources
SPATA22(3)
0.009 0.500 1.48e-2 1.64e-2 ✓ sig. —
Intellectual developmental disorder dysmorphic ptosis Spermatogenic failure
1 gene
Show details
1 of 1 corroborated by 2+ sources
RPL10L(4)
0.009 0.500 1.48e-2 1.64e-2 ✓ sig. —
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development Premature ovarian failure
1 gene
Show details
PNPLA7(1)
0.009 0.500 1.48e-2 1.64e-2 ✓ sig. —
Cerebellar ataxia Neuroocular syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DAGLA(2)
0.009 0.500 1.48e-2 1.64e-2 ✓ sig. —

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