# GeDiPNet Cluster 218 -- Pairs Within Cluster -- generated 2026-10-07 14:36:39
# Similarity: Jaccard index on shared curated genes (disease_gdp). Significance: upper-tail hypergeometric test, Benjamini-Hochberg FDR-corrected across all tested pairs. See scripts/build_related.php on gedipnet.bicnirrh.res.in. Data as of: 2026-10-07 17:17:46.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Scapuloperoneal spinal muscular atrophy	TRPV4-related bone disorder	0.50000	1	6.494e-5	2.317e-4
Parastremmatic dwarfism	TRPV4-related bone disorder	0.50000	1	6.494e-5	2.317e-4
Parastremmatic dwarfism	Scapuloperoneal spinal muscular atrophy	0.50000	1	6.494e-5	2.317e-4
Digital arthropathy-brachydactyly, familial	TRPV4-related bone disorder	0.50000	1	6.494e-5	2.317e-4
Brachyrachia	Congenital benign spinal muscular atrophy	0.50000	1	6.494e-5	2.317e-4
Brachyrachia	Digital arthropathy-brachydactyly, familial	0.50000	1	6.494e-5	2.317e-4
Brachyrachia	Parastremmatic dwarfism	0.50000	1	6.494e-5	2.317e-4
Brachyrachia	Scapuloperoneal spinal muscular atrophy	0.50000	1	6.494e-5	2.317e-4
Brachyrachia	TRPV4-related bone disorder	0.50000	1	6.494e-5	2.317e-4
Congenital benign spinal muscular atrophy	Digital arthropathy-brachydactyly, familial	0.50000	1	6.494e-5	2.317e-4
Congenital benign spinal muscular atrophy	Parastremmatic dwarfism	0.50000	1	6.494e-5	2.317e-4
Congenital benign spinal muscular atrophy	Scapuloperoneal spinal muscular atrophy	0.50000	1	6.494e-5	2.317e-4
Congenital benign spinal muscular atrophy	TRPV4-related bone disorder	0.50000	1	6.494e-5	2.317e-4
Digital arthropathy-brachydactyly, familial	Parastremmatic dwarfism	0.50000	1	6.494e-5	2.317e-4
Digital arthropathy-brachydactyly, familial	Scapuloperoneal spinal muscular atrophy	0.50000	1	6.494e-5	2.317e-4
Brachyolmia	Brachyrachia	0.25000	1	1.948e-4	5.325e-4
Brachyolmia	Scapuloperoneal spinal muscular atrophy	0.25000	1	1.948e-4	5.325e-4
Brachyolmia	Parastremmatic dwarfism	0.25000	1	1.948e-4	5.325e-4
Brachyolmia	Digital arthropathy-brachydactyly, familial	0.25000	1	1.948e-4	5.325e-4
Brachyolmia	Congenital benign spinal muscular atrophy	0.25000	1	1.948e-4	5.325e-4
Congenital benign spinal muscular atrophy	Urination disorders	0.20000	1	2.598e-4	6.484e-4
Brachyrachia	Urination disorders	0.20000	1	2.598e-4	6.484e-4
Digital arthropathy-brachydactyly, familial	Urination disorders	0.20000	1	2.598e-4	6.484e-4
Parastremmatic dwarfism	Urination disorders	0.20000	1	2.598e-4	6.484e-4
Scapuloperoneal spinal muscular atrophy	Urination disorders	0.20000	1	2.598e-4	6.484e-4
