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: C0262395
Disease: Borderline hypertension
Borderline hypertension 		3 0 1 0.33 0 0
CUI: C4016314
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO 		3 0 1 0.33 0 0
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal 		6 0 1 0.17 0 0
CUI: C4021523
Disease: Upper limb amyotrophy
Upper limb amyotrophy 		9 0 1 0.11 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 1 9.1E-02 0 0
CUI: C0033790
Disease: Pseudobulbar Palsy
Pseudobulbar Palsy 		13 0 1 7.7E-02 0 0
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting 		13 0 1 7.7E-02 0 0
CUI: C1843505
Disease: Degeneration of anterior horn cells
Degeneration of anterior horn cells 		15 0 1 6.7E-02 0 0
CUI: C4024921
Disease: Lower limb amyotrophy
Lower limb amyotrophy 		19 0 1 5.3E-02 0 0
CUI: C0043020
Disease: Wallerian Degeneration
Wallerian Degeneration 		21 0 1 4.8E-02 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 1 4.8E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 1 4.3E-02 0 0
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism 		26 0 1 3.8E-02 0 0
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy 		28 0 1 3.6E-02 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes 		28 0 1 3.6E-02 0 0
CUI: C1698196
Disease: Muscle Weakness Upper Limb
Muscle Weakness Upper Limb 		29 0 1 3.4E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 1 3.0E-02 0 0
CUI: C0038506
Disease: Stuttering
Stuttering 		34 0 1 2.9E-02 0 0
CUI: C4022588
Disease: Fatigable weakness of swallowing muscles
Fatigable weakness of swallowing muscles 		39 0 1 2.6E-02 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 1 2.1E-02 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 2.0E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 1 1.8E-02 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 1 1.7E-02 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 1 1.7E-02 0 0
CUI: C0522224
Disease: Paralysed
Paralysed 		68 0 1 1.5E-02 0 0