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
Autoimmune thrombocytopenic purpura Juvenile parkinsonism
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAJC6(3)
0.037 0.333 4.67e-3 5.79e-3 ✓ sig. —
Hemorrhage Juvenile parkinsonism
1 gene
Show details
1 of 1 corroborated by 2+ sources
PODXL(4)
0.037 0.333 4.67e-3 5.79e-3 ✓ sig. —
Autoimmune thrombocytopenic purpura Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DNAJC6(2)
0.037 0.333 4.67e-3 5.79e-3 ✓ sig. —
Hereditary atrial fibrillation Throat disease
1 gene
Show details
1 of 1 corroborated by 2+ sources
GATA5(2)
0.037 0.333 4.67e-3 5.79e-3 ✓ sig. —
Benign adult familial myoclonic epilepsy Myoclonic epilepsy
1 gene
Show details
1 of 1 corroborated by 2+ sources
SAMD12(2)
0.037 0.333 4.67e-3 5.79e-3 ✓ sig. —
Developmental delay with or without intellectual or behavioral abnormalities syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
TAOK1(4)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Dubowitz syndrome syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
NSUN2(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Duplication 15q11-q13 syndrome
1 gene
Show details
AUTS2(1)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Ventricular fibrillation
1 gene
Show details
LIPT2(1)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
17q24.2 microdeletion syndrome syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
BPTF(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Anosmia Moyamoya angiopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
TENM1(2)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Proliferative diabetic retinopathy Temple syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
DLK1(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Cone rod dystrophy and hearing loss Moyamoya angiopathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
CEP78(5)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Congenital anosmia Moyamoya angiopathy
1 gene
Show details
TENM1(1)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Microphthalmia with retinitis pigmentosa and ocular anomalies Microphthalmos
1 gene
Show details
1 of 1 corroborated by 2+ sources
MFRP(2)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. Cluster 56 →
Distal hereditary motor neuropathy Testis atrophy
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLEKHG5(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Cystic leukoencephalopathy Smooth surface dental caries
1 gene
Show details
1 of 1 corroborated by 2+ sources
RNASET2(4)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay Ocular anomalies with axonal neuropathy and developmental delay
1 gene
Show details
1 of 1 corroborated by 2+ sources
ATAD3A(2)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Microphthalmos Oculoauricular syndrome
1 gene
Show details
1 of 1 corroborated by 2+ sources
HMX1(7)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Oculopharyngeal muscular dystrophy T-cell leukemia-lymphoma
1 gene
Show details
1 of 1 corroborated by 2+ sources
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Distal hereditary motor neuropathy Odontochondrodysplasia 2 with hearing loss and diabetes
1 gene
Show details
1 of 1 corroborated by 2+ sources
PLEKHG5(5)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Intellectual developmental disorder dysmorphic microcephaly syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
CTCF(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Cerebral folate deficiency Ocular hypotension
1 gene
Show details
CIC(1)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —
Charcot-Marie-Tooth disease type 2 Distal hereditary motor neuropathy
1 gene
Show details
1 of 1 corroborated by 2+ sources
NEFL(2)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. Cluster 15 →
Peho syndrome syndromic intellectual disability
1 gene
Show details
1 of 1 corroborated by 2+ sources
KIF1A(3)
0.026 0.500 4.67e-3 5.79e-3 ✓ sig. —

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