# GeDiPNet Cluster 105 -- Pairs Within Cluster -- generated 2026-10-07 06:25:47
# 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: 2026-10-07 03:00:13.
Disease A	Disease B	Similarity Score	Shared Genes	P-value	FDR Q-value
Deafness with congenital onychodystrophy	Doors syndrome	0.66667	2	8.436e-9	7.203e-8
Deafness with congenital onychodystrophy	Digitrenocerebral syndrome	0.50000	2	2.531e-8	2.035e-7
Digitrenocerebral syndrome	Doors syndrome	0.50000	2	2.531e-8	2.035e-7
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	0.50000	1	6.494e-5	2.342e-4
Ataxia with polyneuropathy	Periodic paralysis	0.33333	1	1.299e-4	3.898e-4
Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	Periodic paralysis	0.33333	1	1.299e-4	3.898e-4
Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	Infantile myoclonic epilepsy	0.33333	1	1.299e-4	3.898e-4
Doors syndrome	Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	0.33333	1	1.299e-4	3.898e-4
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Periodic paralysis	0.33333	1	1.299e-4	3.898e-4
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Infantile myoclonic epilepsy	0.33333	1	1.299e-4	3.898e-4
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Doors syndrome	0.33333	1	1.299e-4	3.898e-4
Deafness-onychodystrophy syndrome	Doors syndrome	0.33333	1	1.299e-4	3.898e-4
Deafness with congenital onychodystrophy	Deafness-onychodystrophy syndrome	0.33333	1	1.299e-4	3.898e-4
Deafness with congenital onychodystrophy	Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	0.33333	1	1.299e-4	3.898e-4
Deafness with congenital onychodystrophy	Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	0.33333	1	1.299e-4	3.898e-4
Deafness-onychodystrophy syndrome	Zimmermann-laband syndrome	0.25000	1	1.948e-4	5.278e-4
Deafness-onychodystrophy syndrome	Digitrenocerebral syndrome	0.25000	1	1.948e-4	5.278e-4
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Digitrenocerebral syndrome	0.25000	1	1.948e-4	5.278e-4
Digitrenocerebral syndrome	Focal epilepsy-intellectual disability-cerebro-cerebellar malformation	0.25000	1	1.948e-4	5.278e-4
Doors syndrome	Periodic paralysis	0.25000	1	2.598e-4	6.403e-4
Deafness with congenital onychodystrophy	Infantile myoclonic epilepsy	0.25000	1	2.598e-4	6.403e-4
Doors syndrome	Infantile myoclonic epilepsy	0.25000	1	2.598e-4	6.403e-4
Infantile myoclonic epilepsy	Periodic paralysis	0.25000	1	2.598e-4	6.403e-4
Deafness with congenital onychodystrophy	Periodic paralysis	0.25000	1	2.598e-4	6.403e-4
Ataxia with polyneuropathy	Mitochondrial myopathy with sideroblastic anemia	0.20000	1	2.598e-4	6.403e-4
Deafness with congenital onychodystrophy	Zimmermann-laband syndrome	0.20000	1	3.896e-4	8.521e-4
Doors syndrome	Zimmermann-laband syndrome	0.20000	1	3.896e-4	8.521e-4
Mitochondrial myopathy with sideroblastic anemia	Periodic paralysis	0.16667	1	5.195e-4	1.041e-3
Encephalopathy due to mitochondrial and peroxisomal fission defect	Mitochondrial myopathy with sideroblastic anemia	0.16667	1	5.195e-4	1.041e-3