# GeDiPNet Cluster 492 -- Member Diseases -- generated 2026-10-20 00:02:38
# Cluster grouping: label propagation over disease_related's top-5-per-disease shared-gene similarity graph. Cluster size: 6 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
Fontaine progeroid syndrome	5	5	2
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive	4	4	1
Progressive external ophthalmoplegia with mitochondrial dna deletions 3	4	4	1
Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2	4	4	1
Severe early-onset mitochondrial disease and loss of mitochondrial dna copy number	4	4	1
Hypertrichosis, progeroid appearance, and mitochondrial dysfunction (gorlin-chaudhry-moss syndrome )	1	1	1