# GeDiPNet Shared-Gene Disease Pairs -- generated 2026-10-09 19:03:10
# Similarity: Jaccard index on shared curated genes (disease_gdp). Significance: upper-tail hypergeometric test (P(X>=k)), Benjamini-Hochberg FDR-corrected across all tested pairs. Corroborated Shared Genes: count of shared genes backed by >=2 distinct disease_gdp.main_source values combined across both diseases (e.g. GWAS-backed for one, ClinVar-backed for the other still counts); Shared Gene Names lists each gene's own source count in parentheses. Overlap Coefficient: shared genes / MIN(each disease's own total gene count) -- complements the Jaccard-based Similarity Score by showing how much of the SMALLER disease's entire known gene-set is covered by this pair, which Jaccard (dividing by the union) can understate. Shared Cluster: cluster id if both diseases fall in the same label-propagation cluster (scripts/build_disease_clusters.php), blank otherwise. See scripts/build_related.php on gedipnet.bicnirrh.res.in. Data as of: 2026-10-09 03:00:13. Filters applied: disease name contains "Cerebellar ataxia with deafness and narcolepsy" (5 matching pairs).
Disease A	Disease B	Shared Genes	Corroborated Shared Genes	Shared Gene Names	Similarity Score	Overlap Coefficient	P-value	FDR Q-value	Shared Cluster
Cerebellar ataxia with deafness and narcolepsy	Cerebellar ataxia, deafness, and narcolepsy	1	1	DNMT1 (7)	0.50000	1.00000	6.494e-5	2.329e-4	
Cerebellar ataxia with deafness and narcolepsy	Dominantly inherited sensory neuropathy	1	1	DNMT1 (5)	0.25000	1.00000	1.948e-4	5.350e-4	
Cerebellar ataxia with deafness and narcolepsy	Cerebral atrophy	1	1	DNMT1 (5)	0.12500	1.00000	4.546e-4	9.721e-4	
Beckwith-wiedemann syndrome	Cerebellar ataxia with deafness and narcolepsy	1	1	DNMT1 (5)	0.09091	1.00000	6.494e-4	1.241e-3	
Cerebellar ataxia with deafness and narcolepsy	Deglutition disorder	1	1	DNMT1 (5)	0.08333	1.00000	7.144e-4	1.335e-3