# GeDiPNet Shared-Gene Disease Pairs -- generated 2026-10-10 06:58:34
# 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: 2026-10-10 03:00:13. Filters applied: disease name contains "inborn disorder of cobalamin metabolism and transport" (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
inborn disorder of cobalamin metabolism and transport	Methylmalonic acidemia	1	1	MMADHC (7)	0.03571	1.00000	1.753e-3	2.609e-3	
inborn disorder of cobalamin metabolism and transport	Intracellular cobalamin metabolism disorder	1	1	MMADHC (2)	0.10000	1.00000	5.845e-4	1.156e-3	
Cobalamin c disease	inborn disorder of cobalamin metabolism and transport	1	1	MMADHC (2)	0.12500	1.00000	4.546e-4	9.726e-4	
Homocystinuria with megaloblastic anemia	inborn disorder of cobalamin metabolism and transport	1	1	MMADHC (3)	0.20000	1.00000	2.598e-4	6.509e-4	
Cobalamin metabolism disorder	inborn disorder of cobalamin metabolism and transport	1	1	MMADHC (2)	0.50000	1.00000	6.494e-5	2.331e-4