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: C1262117
Disease: Fungal keratitis
Fungal keratitis 		21 0 8 0.15 0 0
CUI: C0278147
Disease: Radicular pain
Radicular pain 		23 0 8 0.14 0 0
CUI: C2348101
Disease: Destructive Arthritis
Destructive Arthritis 		23 0 8 0.14 0 0
CUI: C0178782
Disease: Orofacial Pain
Orofacial Pain 		40 0 10 0.14 0 0
CUI: C0036396
Disease: Sciatica
Sciatica 		24 0 8 0.14 0 0
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		25 0 8 0.14 0 0
CUI: C1849508
Disease: EPILEPSY, PYRIDOXINE-DEPENDENT
EPILEPSY, PYRIDOXINE-DEPENDENT 		25 0 8 0.14 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		10 0 6 0.13 0 0
CUI: C1707446
Disease: Columnar Cell Hyperplasia of the Breast
Columnar Cell Hyperplasia of the Breast 		38 0 9 0.13 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		30 0 8 0.13 0 0
CUI: C0409818
Disease: Chronic Infantile Neurological, Cutaneous, and Articular Syndrome
Chronic Infantile Neurological, Cutaneous, and Articular Syndrome 		30 0 8 0.13 0 0
CUI: C1290807
Disease: Diarrheal disorder
Diarrheal disorder 		32 0 8 0.12 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 5 0.12 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 5 0.12 0 0
CUI: C0751434
Disease: Classical phenylketonuria
Classical phenylketonuria 		42 0 9 0.12 0 0
CUI: C1861303
Disease: SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)
SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder) 		33 0 8 0.12 0 0
CUI: C0268390
Disease: Muckle-Wells Syndrome
Muckle-Wells Syndrome 		34 0 8 0.12 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 13 0.12 0 0
CUI: C1857941
Disease: Brooke-Spiegler syndrome
Brooke-Spiegler syndrome 		45 0 9 0.12 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 5 0.12 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 5 0.12 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 5 0.12 0 0
CUI: C0877430
Disease: Asthma chronic
Asthma chronic 		36 0 8 0.12 0 0
CUI: C0005129
Disease: Bernard-Soulier Syndrome
Bernard-Soulier Syndrome 		46 0 9 0.12 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 0 9 0.12 0 0