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: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
145 0 1 3.1E-03 0 0
CUI: C0270846
Disease: Epileptic drop attack
Epileptic drop attack
143 0 1 3.1E-03 0 0
CUI: C0149958
Disease: Complex partial seizures
Complex partial seizures
140 0 1 3.1E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
136 0 1 3.1E-03 0 0
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
135 0 1 3.2E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 3.2E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay
130 0 1 3.2E-03 0 0
Amyotrophic Lateral Sclerosis, Familial
130 0 1 3.2E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
123 0 1 3.3E-03 0 0
CUI: C4317123
Disease: Myoclonic Seizures
Myoclonic Seizures
123 0 1 3.3E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 3.3E-03 0 0
CUI: C0013371
Disease: Shigella Infections
Shigella Infections
121 0 1 3.3E-03 0 0
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis
121 0 1 3.3E-03 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 1 3.3E-03 0 0
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media
120 0 1 3.3E-03 0 0
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis
118 0 1 3.3E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
118 0 1 3.3E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 1 3.3E-03 0 0
CUI: C0751494
Disease: Convulsive Seizures
Convulsive Seizures
117 0 1 3.3E-03 0 0
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy
113 0 1 3.4E-03 0 0
CUI: C3160909
Disease: Autoimmune arthritis
Autoimmune arthritis
113 0 1 3.4E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 3.4E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 3.4E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder)
109 0 1 3.4E-03 0 0
CUI: C0270844
Disease: Tonic Seizures
Tonic Seizures
108 0 1 3.4E-03 0 0