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
DDOST-congenital disorder of glycosylation Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
DDOST(2)
0.001 1.000 5.25e-2 5.42e-2 —
Dentici novelli neurodevelopmental syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ZNF526(4)
0.001 1.000 5.25e-2 5.42e-2 —
Developmental delay with behavioral abnormalities Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ADGRL1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Developmental delay with overweight and facial dysmorphism Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SRRM2(5)
0.001 1.000 5.25e-2 5.42e-2 —
Diffuse cerebral and cerebellar atrophy–intractable seizures–progressive microcephaly syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
QARS1(4)
0.001 1.000 5.25e-2 5.42e-2 —
Early-onset epilepsy-intellectual disability-brain anomalies syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
PIGG(4)
0.001 1.000 5.25e-2 5.42e-2 —
Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
OTUD6B(2)
0.001 1.000 5.25e-2 5.42e-2 —
Ectopic thyroid tissue Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
FBXO31(5)
0.001 1.000 5.25e-2 5.42e-2 —
El-hayek-chahrour neurodevelopmental syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
KDM5A(5)
0.001 1.000 5.25e-2 5.42e-2 —
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS4A(4)
0.001 1.000 5.25e-2 5.42e-2 —
Cerebrocostomandibular syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
SNRPB(6)
0.001 1.000 5.25e-2 5.42e-2 —
Chondroblastoma Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
H3-3B(2)
0.001 1.000 5.25e-2 5.42e-2 —
Chopra-amiel-gordon syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ANKRD17(4)
0.001 1.000 5.25e-2 5.42e-2 —
Cimdag syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
VPS4A(3)
0.001 1.000 5.25e-2 5.42e-2 —
Clark-baraitser syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
TRIP12(4)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Giant cell tumor of bone Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
H3-3A(2)
0.001 1.000 5.25e-2 5.42e-2 —
glutamate pyruvate transaminase 2 deficiency Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
GPT2(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
goldberg-shprintzen syndrome Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIFBP(3)
0.001 1.000 5.25e-2 5.42e-2 —
Hemiparkinsonism hemiatrophy syndrome Intellectual developmental disorder
1 gene
Show details
H3-3B(1)
0.001 1.000 5.25e-2 5.42e-2 —
hereditary spastic paraplegia 18 Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
ERLIN2(3)
0.001 1.000 5.25e-2 5.42e-2 —
holoprosencephaly 12 with or without pancreatic agenesis Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
CNOT1(2)
0.001 1.000 5.25e-2 5.42e-2 —
hypomyelinating leukodystrophy 5 Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
HYCC1(3)
0.001 1.000 5.25e-2 5.42e-2 —
hypotonia, infantile, with psychomotor retardation and characteristic facies 2 Intellectual developmental disorder
1 gene
Show details
1 of 1 corroborated by 2+ sources
UNC80(2)
0.001 1.000 5.25e-2 5.42e-2 Cluster 6 →
Gout lesch-nyhan syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HPRT1(3)
0.001 1.000 5.32e-2 5.48e-2 —
Gout leukoencephalopathy with vanishing white matter 4
1 gene
Show details
1 of 1 corroborated by 2+ sources
EIF2B4(2)
0.001 1.000 5.32e-2 5.48e-2 —

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