# GeDiPNet Cluster 2 -- Member Diseases -- generated 2026-10-07 19:43:00
# Cluster grouping: label propagation over disease_related's top-5-per-disease shared-gene similarity graph. Cluster size: 57 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: 2026-10-07 03:15:01.
Disease	Connections in Cluster	Significant Partners (q<0.05)	Curated Genes
Major depressive disorder	19	17	1960
Schizophrenia	17	12	2541
Diabetes mellitus type 2	17	9	3080
Metabolic syndrome	13	11	1303
Bipolar disorder	13	9	1220
Attention deficit hyperactivity disorder	11	10	1105
Alzheimer disease	10	8	2218
Insomnia	10	8	1079
Obesity	9	8	1194
Parkinson disease	9	8	529
Substance abuse	9	8	516
Scoliosis	9	7	1033
Color vision deficiency	8	8	966
Osteoarthritis	8	8	730
Dementia	8	7	590
Anxiety disorder	7	7	146
Mood disorder	7	7	298
Neurotic disorder	7	7	435
Post-traumatic stress disorder	7	7	203
Depression	6	6	279
Autism	6	4	1463
Bipolar depression	5	5	105
Oligodendroglioma	5	5	559
Cannabis abuse	4	4	116
Gastroesophageal reflux disease	4	4	279
Irritable bowel syndrome	4	4	134
Ear disorder	4	1	2
retinitis pigmentosa 18	4	1	1
Oculocerebrodental syndrome	4	0	1
Panic disorder	3	3	34
Willis-ekbom disease	3	3	191
3-methylcrotonyl-coa carboxylase deficiency	3	1	2
Birk-aharoni syndrome	3	0	2
opsismodysplasia	3	0	1
Gout	2	2	819
Pemphigus foliaceus	2	2	1
Alopecia-neurological defects-endocrinopathy syndrome	2	1	1
Craniolenticulosutural dysplasia	2	1	1
Partial deletion of short arm of chromosome 3	2	1	1
SNUPN-related muscular dystrophy with or without multi-system involvement	2	1	1
inherited interstitial lung disease	2	1	1
Auroneurodental syndrome	2	0	2
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	1	1	1
Congenital lactase deficiency	1	1	1
Developmental delay with language and ocular abnormalities	1	1	2
Diabetes deafness developmental delay and short stature syndrome	1	1	1
Patellar tendinitis	1	1	2
Sedoheptulokinase deficiency	1	1	1
Deafness, y-linked	1	0	1
Glyoxalase ii deficiency	1	0	1
Phosphoribosylaminoimidazole carboxylase deficiency	1	0	1
Vacuolar neuromyopathy	1	0	1
Vibratory urticaria	1	0	1
Warsaw breakage syndrome	1	0	1
hydroxyprolinemia	1	0	1
pterin-4 alpha-carbinolamine dehydratase 1 deficiency	1	0	1
siddiqi syndrome	1	0	1