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: C1960561
Disease: Hemidystonia
Hemidystonia 		1 0 1 0.25 0 0
CUI: C4016100
Disease: FMO3 ACTIVITY, DECREASED
FMO3 ACTIVITY, DECREASED 		1 1 1 0.25 1 5.9E-02
CUI: C0598106
Disease: Encephalomyelopathy
Encephalomyelopathy 		2 0 1 0.20 0 0
CUI: C0751645
Disease: Human Transmissible Spongiform Encephalopathies, Inherited
Human Transmissible Spongiform Encephalopathies, Inherited 		2 0 1 0.20 0 0
CUI: C1291512
Disease: Beta-Ureidopropionase Deficiency
Beta-Ureidopropionase Deficiency 		2 0 1 0.20 0 0
CUI: C2677535
Disease: Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 		2 0 1 0.20 0 0
CUI: C0007020
Disease: Carbon Monoxide Poisoning
Carbon Monoxide Poisoning 		4 0 1 0.14 0 0
CUI: C0393489
Disease: Vacuolar myelopathy
Vacuolar myelopathy 		4 0 1 0.14 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 0 1 0.14 0 0
CUI: C3495421
Disease: Chromosome 18q syndrome
Chromosome 18q syndrome 		4 0 1 0.14 0 0
CUI: C0809935
Disease: Chromosome 18, trisomy 18q
Chromosome 18, trisomy 18q 		5 0 1 0.12 0 0
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		6 0 1 0.11 0 0
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		6 0 1 0.11 0 0
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 1 0.11 0 0
CUI: C0339358
Disease: Infantile cataract
Infantile cataract 		6 0 1 0.11 0 0
CUI: C0432443
Disease: Deletion of long arm of chromosome 18
Deletion of long arm of chromosome 18 		6 0 1 0.11 0 0
CUI: C0270780
Disease: Degenerative myelopathy
Degenerative myelopathy 		7 0 1 1.0E-01 0 0
CUI: C0948786
Disease: Blanching
Blanching 		7 0 1 1.0E-01 0 0
CUI: C0393665
Disease: Multiple Sclerosis, Chronic Progressive
Multiple Sclerosis, Chronic Progressive 		8 0 1 9.1E-02 0 0
CUI: C1301721
Disease: Neurological morbidity
Neurological morbidity 		8 0 1 9.1E-02 0 0
CUI: C0011304
Disease: Demyelination
Demyelination 		9 0 1 8.3E-02 0 0
CUI: C0342500
Disease: Adrenal mass
Adrenal mass 		9 0 1 8.3E-02 0 0
CUI: C0553604
Disease: Myotonic Disorders
Myotonic Disorders 		9 0 1 8.3E-02 0 0
CUI: C2350037
Disease: Clinically Isolated Syndrome, CNS Demyelinating
Clinically Isolated Syndrome, CNS Demyelinating 		9 0 1 8.3E-02 0 0
CUI: C4554010
Disease: Isomerism (body)
Isomerism (body) 		9 0 1 8.3E-02 0 0