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: C0342422
Disease: Pituitary gland enlarged
Pituitary gland enlarged 		8 0 4 0.12 0 0
CUI: C0221184
Disease: Bitemporal Hemianopia
Bitemporal Hemianopia 		9 0 4 0.12 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 12 0.12 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 4 0.11 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 4 0.11 0 0
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum 		12 0 4 0.11 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum 		55 0 8 0.11 0 0
CUI: C1832276
Disease: Thenar muscle weakness
Thenar muscle weakness 		3 0 3 0.10 0 0
CUI: C1832277
Disease: First dorsal interossei muscle weakness
First dorsal interossei muscle weakness 		3 0 3 0.10 0 0
CUI: C1832278
Disease: First dorsal interossei muscle atrophy
First dorsal interossei muscle atrophy 		3 0 3 0.10 0 0
CUI: C1832279
Disease: Cold-induced hand cramps
Cold-induced hand cramps 		3 0 3 0.10 0 0
CUI: C4021031
Disease: Abnormal motor nerve conduction velocity
Abnormal motor nerve conduction velocity 		3 0 3 0.10 0 0
CUI: C4024895
Disease: Atrophy/Degeneration involving the caudate nucleus
Atrophy/Degeneration involving the caudate nucleus 		3 0 3 0.10 0 0
CUI: C4021655
Disease: Abnormality of the sense of smell
Abnormality of the sense of smell 		14 0 4 0.10 0 0
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy 		15 0 4 1.0E-01 0 0
CUI: C1853141
Disease: Slow decrease in visual acuity
Slow decrease in visual acuity 		27 0 5 9.8E-02 0 0
CUI: C0338591
Disease: Amnesia, Transient Global
Amnesia, Transient Global 		16 0 4 9.8E-02 0 0
CUI: C3551915
Disease: MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO 		5 0 3 9.7E-02 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 5 9.6E-02 0 0
CUI: C1333989
Disease: Familial meningioma
Familial meningioma 		6 0 3 9.4E-02 0 0
CUI: C1837251
Disease: Basal ganglia cysts
Basal ganglia cysts 		6 0 3 9.4E-02 0 0
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 0 3 9.4E-02 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 6 9.4E-02 0 0
CUI: C4022798
Disease: Abnormal brain FDG positron emission tomography
Abnormal brain FDG positron emission tomography 		18 0 4 9.3E-02 0 0
CUI: C4025669
Disease: Decreased circulating ACTH level
Decreased circulating ACTH level 		18 0 4 9.3E-02 0 0