# GeDiPNet Cluster 109 -- Pairs Within Cluster -- generated 2026-10-07 00:38:55
# 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 03:00:12.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Caudal regression syndrome	Sacral defect	0.50000	2	2.531e-8	2.035e-7
Congenital exomphalos	Congenital omphalocele	0.25000	2	1.772e-7	1.249e-6
Caudal regression syndrome	Neural tube defects, susceptibility to	0.28571	2	2.530e-7	1.745e-6
Auditory system disease	Vascular brain injury	0.08333	2	4.202e-5	2.026e-4
15q13.3 microdeletion syndrome	Congenital exomphalos	0.25000	1	2.598e-4	6.403e-4
Congenital exomphalos	Currarino syndrome	0.25000	1	2.598e-4	6.403e-4
Congenital exomphalos	Sacral defect	0.25000	1	2.598e-4	6.403e-4
Currarino syndrome	Sacral defect	0.25000	1	2.598e-4	6.403e-4
Neural tube defects, susceptibility to	Yellow nail syndrome	0.16667	1	3.247e-4	7.577e-4
Caudal regression syndrome	Congenital exomphalos	0.20000	1	3.896e-4	8.521e-4
Caudal regression syndrome	Currarino syndrome	0.20000	1	3.896e-4	8.521e-4
Neural tube defects, susceptibility to	Sacral defect	0.14286	1	6.494e-4	1.219e-3
15q13.3 microdeletion syndrome	Congenital omphalocele	0.11111	1	9.090e-4	1.557e-3
Congenital omphalocele	Sacral defect	0.11111	1	9.090e-4	1.557e-3
Congenital omphalocele	Currarino syndrome	0.11111	1	9.090e-4	1.557e-3
autosomal dominant cerebellar ataxia	Vascular brain injury	0.06667	1	9.092e-4	1.557e-3
Caudal regression syndrome	Congenital omphalocele	0.10000	1	1.363e-3	2.129e-3
Congenital exomphalos	Vascular brain injury	0.06250	1	1.818e-3	2.662e-3
Currarino syndrome	Vascular brain injury	0.06250	1	1.818e-3	2.662e-3
Sacral defect	Vascular brain injury	0.06250	1	1.818e-3	2.662e-3