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Table 2 Disease network top 20 significant connections CPBA

From: Cluster and propensity based approximation of a network

  Disease 1 Disease 2 C1 C2 −Log10(P)
1 Zellweger syndrome Adrenoleukodystrophy 14 14 8.57
2 Muscular dystrophy-dystroglycanopathy (limb-girdle) Muscular dystrophy-dystroglycanopathy (congenital) 2 2 7.05
3 Ullrich congenital muscular dystrophy Bethlem myopathy 14 14 6.48
4 Iminoglycinuria Hyperglycinuria 14 14 6.48
5 Alport syndrome Hematuria 14 14 5.31
6 Colorblindness Blue cone monochromacy 14 14 5.31
7 Refsum disease Zellweger syndrome 14 14 5.05
8 Usher syndrome Retinitis pigmentosa 8 6 5.04
9 Seckel syndrome Microcephaly 14 14 4.96
10 Leukoencephalopathy with vanishing white matter Ovarioleukodystrophy 14 14 4.96
11 Omenn syndrome Severe combined immunodeficiency 14 14 4.90
12 Tuberous sclerosis Lymphangioleio-myomatosis 14 14 4.60
13 Cone-rod dystrophy Macular degeneration 6 10 4.60
14 Bronchiectasis with or without elevated sweat chloride Pseudohypoaldoste-ronism 11 11 4.47
15 Leri-Weill dyschondrosteosis Langer mesomelic dysplasia 14 14 4.10
16 Multiple pterygium syndrome Myasthenic syndrome 14 14 4.00
17 Craniofacial-deafness-hand syndrome Waardenburg syndrome 3 11 3.77
18 Nicotine addiction Epilepsy 3 8 3.76
19 Hirschsprung disease Pheochromocytoma 11 2 3.70
20 Langer mesomelic dysplasia Short stature 14 14 3.62