# GeDiPNet Cluster 658 -- Pairs Within Cluster -- generated 2026-10-21 23:30:53
# 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: 2026-10-22 03:00:19.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Neurodevelopmental disorder with distinct white matter changes	Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language	0.50000	1	6.457e-5	1.985e-4
Neurodevelopmental disorder with distinct white matter changes	Renu syndrome	0.50000	1	6.457e-5	1.985e-4
Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language	Renu syndrome	0.50000	1	6.457e-5	1.985e-4
Neurodevelopmental disorder with distinct white matter changes	Neurodevelopmental disorder with microcephaly and seizures	0.25000	1	1.937e-4	4.415e-4
Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language	Neurodevelopmental disorder with microcephaly and seizures	0.25000	1	1.937e-4	4.415e-4
Neurodevelopmental disorder with microcephaly and seizures	Neurodevelopmental disorder with poor growth and skeletal anomalies	0.25000	1	1.937e-4	4.415e-4
Neurodevelopmental disorder with microcephaly and seizures	Renu syndrome	0.25000	1	1.937e-4	4.415e-4