# GeDiPNet Cluster 630 -- Member Diseases -- generated 2026-10-20 00:02:41
# Cluster grouping: label propagation over disease_related's top-5-per-disease shared-gene similarity graph. Cluster size: 5 diseases. Sorted by connections within the cluster (most central first). Connections/partners count deduplicated disease pairs; significant = FDR q < 0.05. See scripts/build_disease_clusters.php on gedipnet.bicnirrh.res.in. Data as of: 2026-10-20 03:15:01.
Disease	Connections in Cluster	Significant Partners (q<0.05)	Curated Genes
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome	3	3	2
Lipoyltransferase deficiency	3	3	3
Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities	2	2	1
Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase	1	1	1
Progressive childhood encephalopathy and golgi dysfunction	1	1	1