# GeDiPNet Shared-Gene Disease Pairs -- generated 2026-10-13 20:16:56
# 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: 2026-10-13 03:00:13. Filters applied: disease name contains "Yemenite deaf-blind hypopigmentation syndrome" (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
Growth hormone deficiency	Yemenite deaf-blind hypopigmentation syndrome	1	0	SOX10 (1)	0.02857	1.00000	2.208e-3	3.113e-3	
Waardenburg syndrome	Yemenite deaf-blind hypopigmentation syndrome	1	1	SOX10 (8)	0.07143	1.00000	8.443e-4	1.499e-3	
Waardenburg-shah syndrome	Yemenite deaf-blind hypopigmentation syndrome	1	1	SOX10 (3)	0.20000	1.00000	2.598e-4	6.509e-4	
Deaf blind hypopigmentation syndrome	Yemenite deaf-blind hypopigmentation syndrome	1	1	SOX10 (2)	0.50000	1.00000	6.494e-5	2.331e-4	
Waardenburg syndrome type 4C	Yemenite deaf-blind hypopigmentation syndrome	1	1	SOX10 (2)	0.50000	1.00000	6.494e-5	2.331e-4