# GeDiPNet Cluster 91 -- Pairs Within Cluster -- generated 2026-10-08 09:07:22
# 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: 2026-10-08 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	1.932e-7
Congenital exomphalos	Congenital omphalocele	0.25000	2	1.772e-7	1.185e-6
Caudal regression syndrome	Neural tube defects, susceptibility to	0.28571	2	2.530e-7	1.658e-6
Auditory system disease	Vascular brain injury	0.08333	2	4.202e-5	1.921e-4
15q13.3 microdeletion syndrome	Congenital exomphalos	0.25000	1	2.598e-4	6.484e-4
Congenital exomphalos	Currarino syndrome	0.25000	1	2.598e-4	6.484e-4
Congenital exomphalos	Sacral defect	0.25000	1	2.598e-4	6.484e-4
Currarino syndrome	Sacral defect	0.25000	1	2.598e-4	6.484e-4
Neural tube defects, susceptibility to	Yellow nail syndrome	0.16667	1	3.247e-4	7.680e-4
Caudal regression syndrome	Congenital exomphalos	0.20000	1	3.896e-4	8.637e-4
Caudal regression syndrome	Currarino syndrome	0.20000	1	3.896e-4	8.637e-4
Neural tube defects, susceptibility to	Sacral defect	0.14286	1	6.494e-4	1.239e-3
15q13.3 microdeletion syndrome	Congenital omphalocele	0.11111	1	9.090e-4	1.575e-3
Congenital omphalocele	Sacral defect	0.11111	1	9.090e-4	1.575e-3
Congenital omphalocele	Currarino syndrome	0.11111	1	9.090e-4	1.575e-3
autosomal dominant cerebellar ataxia	Vascular brain injury	0.06667	1	9.092e-4	1.575e-3
Caudal regression syndrome	Congenital omphalocele	0.10000	1	1.363e-3	2.146e-3
Congenital exomphalos	Vascular brain injury	0.06250	1	1.818e-3	2.675e-3
Currarino syndrome	Vascular brain injury	0.06250	1	1.818e-3	2.675e-3
Sacral defect	Vascular brain injury	0.06250	1	1.818e-3	2.675e-3