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: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 1.8E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 1.9E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 1.9E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
156 0 1 1.9E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 2.0E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.0E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 1 2.0E-03 0 0
Sensorineural hearing loss, bilateral
117 0 1 2.0E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness
112 0 1 2.0E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
104 0 1 2.1E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
100 0 1 2.1E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 2.1E-03 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
94 0 1 2.1E-03 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy
93 0 1 2.1E-03 0 0
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
92 0 1 2.1E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
90 0 1 2.1E-03 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers
88 0 1 2.2E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness
87 0 1 2.2E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
86 0 1 2.2E-03 0 0
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia
86 0 1 2.2E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 0 1 2.2E-03 0 0
Respiratory insufficiency due to muscle weakness
85 0 1 2.2E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 2.2E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 2.2E-03 0 0
Autosomal recessive retinitis pigmentosa
82 0 1 2.2E-03 0 0