Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 1 1.9E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose 		70 0 1 1.9E-03 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection 		69 0 1 1.9E-03 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 1 1.9E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.9E-03 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 1 1.9E-03 0 0
CUI: C0266292
Disease: Congenital anomaly of the kidney
Congenital anomaly of the kidney 		63 0 1 1.9E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 1.9E-03 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis 		62 0 1 1.9E-03 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		61 0 1 2.0E-03 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		60 0 1 2.0E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 2.0E-03 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve 		59 0 1 2.0E-03 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 1 2.0E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 535 1 2.0E-03 2 2.7E-03
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 2.0E-03 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 1 2.0E-03 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum 		55 0 1 2.0E-03 0 0
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		55 0 1 2.0E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 2.0E-03 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 108 1 2.0E-03 1 3.1E-03
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 2.0E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 2.0E-03 0 0
CUI: C0338474
Disease: Central nervous system demyelination
Central nervous system demyelination 		52 0 1 2.0E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 2.0E-03 0 0