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
Desbuquois syndrome Short stature skeletal dysplasia retinal degeneration intellectual disability hearing loss syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
PISD(3)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome spondyloepimetaphyseal dysplasia with joint laxity, type 3
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXOC6B(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome spondyloepimetaphyseal dysplasia, genevieve type
1 gene
Show details
1 of 1 corroborated by 2+ sources
NANS(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome syndactyly-telecanthus-anogenital and renal malformations syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CCNQ(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Brachytelephalangic chondrodysplasia punctata Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ARSL(3)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Calvarial doughnut lesions with bone fragility Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SGMS2(4)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Camptosynpolydactyly Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
BHLHA9(5)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome hand-foot-genital syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HOXA13(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome hyperparathyroidism 2 with jaw tumors
1 gene
Show details
1 of 1 corroborated by 2+ sources
CDC73(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome hyperphosphatasia with intellectual disability syndrome 1
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIGV(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Desbuquois syndrome hypopigmentation, organomegaly, and delayed myelination and development
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN7(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Cataract-neurodevelopmental syndrome Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
FAR1(4)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Cathepsin a-related arteriopathy, strokes, and leukoencephalopathy Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTSA(3)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Cerebellar ataxia, brain abnormalities, and cardiac conduction defects Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
EXOSC5(5)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Cerebrocostomandibular syndrome Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SNRPB(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
chondrodysplasia with joint dislocations, gpapp type Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
BPNT2(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Cleft lip/palate with abnormal thumbs and microcephaly Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
ESCO2(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
Codas syndrome Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
LONP1(6)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
COG1-congenital disorder of glycosylation Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COG1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
COG4-congenital disorder of glycosylation Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
COG4(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
aspartylglucosaminuria Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
AGA(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
autosomal dominant osteopetrosis 2 Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN7(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
autosomal recessive osteopetrosis 4 Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
CLCN7(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
autosomal recessive osteopetrosis 5 Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
OSTM1(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —
autosomal recessive osteopetrosis 8 Desbuquois syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
SNX10(2)
0.002 1.000 3.68e-2 3.87e-2 ✓ sig. —

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