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
Cardiomegaly Isolated anhidrosis
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITPR2(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ITGA3(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Congenital folate absorption defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC46A1(3)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
1 gene
Show details
ITGA3(1)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Congenital phimosis
1 gene
Show details
ITGA3(1)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Malabsorption syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SLC46A1(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia Serrated polyposis
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNF43(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia sessile serrated polyposis cancer syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNF43(2)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Anemia spinocerebellar ataxia, autosomal recessive 31
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATG7(3)
0.012 1.000 5.46e-3 6.63e-3 ✓ sig. —
Developmental delay with short stature and dysmorphic facial features Ventricular septal defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
DPH2(3)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Brain disease Whim syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CXCR2(5)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Hypospadias X-linked myotubular myopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
MAMLD1(6)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Intellectual developmental disorder seizures speech Proteinuria
1 gene
Show details
1 of 1 corroborated by 2+ sources
PAK1(4)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. Cluster 30 →
Fetal erythroblastosis Lupus nephritis
1 gene
Show details
FCGR2A(1)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Craniofacial dysplasia short stature ectodermal anomalies intellectual disability syndrome Ventricular septal defect
1 gene
Show details
1 of 1 corroborated by 2+ sources
DPH2(2)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Brain disease Cystic leukoencephalopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNASET2(5)
0.023 0.500 5.45e-3 6.63e-3 ✓ sig. —
Brachydactyly Chromosome 2q37 deletion syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HDAC4(4)
0.040 0.250 5.44e-3 6.63e-3 ✓ sig. —
Citrullinemia Diabetic angiopathies
1 gene
Show details
1 of 1 corroborated by 2+ sources
ASS1(7)
0.032 0.333 5.45e-3 6.63e-3 ✓ sig. —
Hereditary parkinson disease Juvenile parkinsonism
1 gene
Show details
1 of 1 corroborated by 2+ sources
PODXL(3)
0.032 0.333 5.45e-3 6.63e-3 ✓ sig. Cluster 256 →
Galactosialidosis Hypertriglyceridemia
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLTP(2)
0.032 0.333 5.45e-3 6.63e-3 ✓ sig. —
Hypertriglyceridemia Malignant glioma
1 gene
Show details
1 of 1 corroborated by 2+ sources
LMF1(2)
0.032 0.333 5.45e-3 6.63e-3 ✓ sig. —
Congenital pes cavus hearing loss, autosomal recessive
1 gene
Show details
1 of 1 corroborated by 2+ sources
PTPRQ(2)
0.053 0.143 5.44e-3 6.63e-3 ✓ sig. —
Cardiofaciocutaneous syndrome Corticobasal degeneration
1 gene
Show details
1 of 1 corroborated by 2+ sources
SOS1(3)
0.053 0.143 5.44e-3 6.63e-3 ✓ sig. Cluster 42 →
Adrenal gland neoplasms Corneal disease
1 gene
Show details
TCF4(1)
0.053 0.143 5.44e-3 6.63e-3 ✓ sig. Cluster 222 →
Adrenal gland neoplasms Paranoia
1 gene
Show details
1 of 1 corroborated by 2+ sources
TCF4(2)
0.053 0.143 5.44e-3 6.63e-3 ✓ sig. Cluster 222 →

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