From: Cluster and propensity based approximation of a network
 | Disease 1 | Disease 2 | C1 | C2 | - Log10(P) |
---|---|---|---|---|---|
1 | Muscular dystrophy-dystroglycanopathy (limb-girdle) | Muscular dystrophy-dystroglycanopathy (congenital) | 2 | 2 | 13.31 |
2 | Zellweger syndrome | Adrenoleukodystrophy | 14 | 14 | 12.06 |
3 | Leber congenital amaurosis | Retinitis pigmentosa | 6 | 6 | 10.12 |
4 | Neuropathy | Charcot-Marie-Tooth disease | 12 | 12 | 8.99 |
5 | Blood group | Malaria | 13 | 13 | 8.76 |
6 | Ullrich congenital muscular dystrophy | Bethlem myopathy | 14 | 14 | 8.57 |
7 | Iminoglycinuria | Hyperglycinuria | 14 | 14 | 8.57 |
8 | Usher syndrome | Deafness | 8 | 8 | 8.48 |
9 | Hemolytic uremic syndrome | Macular degeneration | 10 | 10 | 8.24 |
10 | Bronchiectasis with or without elevated sweat chloride | Pseudohypoal-dosteronism | 11 | 11 | 7.75 |
11 | Refsum disease | Zellweger syndrome | 14 | 14 | 7.14 |
12 | Meckel syndrome | Joubert syndrome | 6 | 6 | 7.08 |
13 | Omenn syndrome | Severe combined immunodeficiency | 14 | 14 | 6.99 |
14 | Left ventricular noncompaction | Cardiomyopathy | 12 | 12 | 6.97 |
15 | Mitochondrial complex I deficiency | Leigh syndrome | 2 | 2 | 6.85 |
16 | Alport syndrome | Hematuria | 14 | 14 | 6.70 |
17 | Colorblindness | Blue cone monochromacy | 14 | 14 | 6.70 |
18 | Atrial fibrillation | Long QT syndrome | 2 | 2 | 6.64 |
19 | Cone-rod dystrophy | Retinitis pigmentosa | 6 | 6 | 6.56 |
20 | Microphthalmia with coloboma | Microphthalmia | 6 | 6 | 6.46 |