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: C0233849
Disease: Personality Traits
Personality Traits 		24 0 1 6.2E-04 0 0
CUI: C4021728
Disease: EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation 		24 0 1 6.2E-04 0 0
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency 		24 0 1 6.2E-04 0 0
CUI: C0034642
Disease: Rales
Rales 		23 0 1 6.2E-04 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 1 6.2E-04 0 0
CUI: C0877017
Disease: Generalized tonic-clonic seizures with focal onset
Generalized tonic-clonic seizures with focal onset 		23 0 1 6.2E-04 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 6.2E-04 0 0
CUI: C3163798
Disease: Recurrent lower respiratory tract infection
Recurrent lower respiratory tract infection 		23 0 1 6.2E-04 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 1 6.2E-04 0 0
CUI: C4025797
Disease: Abnormality of prenatal development or birth
Abnormality of prenatal development or birth 		23 0 1 6.2E-04 0 0
CUI: C0010691
Disease: Cystinuria
Cystinuria 		22 0 1 6.2E-04 0 0
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment 		22 0 1 6.2E-04 0 0
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		22 0 1 6.2E-04 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 1 6.2E-04 0 0
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		22 0 1 6.2E-04 0 0
CUI: C0085400
Disease: Neurofibrillary degeneration (morphologic abnormality)
Neurofibrillary degeneration (morphologic abnormality) 		21 0 1 6.2E-04 0 0
CUI: C0149520
Disease: Acute Cholecystitis
Acute Cholecystitis 		21 0 1 6.2E-04 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 1 6.2E-04 0 0
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		21 0 1 6.2E-04 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		21 0 1 6.2E-04 0 0
CUI: C0339985
Disease: Idiopathic bronchiectasis
Idiopathic bronchiectasis 		21 0 1 6.2E-04 0 0
CUI: C1184919
Disease: Thoracic kyphosis
Thoracic kyphosis 		21 0 1 6.2E-04 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 1 6.2E-04 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 1 6.2E-04 0 0
CUI: C1837485
Disease: Flat acetabular roof
Flat acetabular roof 		21 0 1 6.2E-04 0 0