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: C0751716
Disease: Adult Neuroaxonal Dystrophy
Adult Neuroaxonal Dystrophy 		2 0 2 0.29 0 0
CUI: C0751717
Disease: Juvenile Neuroaxonal Dystrophy
Juvenile Neuroaxonal Dystrophy 		2 0 2 0.29 0 0
CUI: C0751718
Disease: Late Infantile Neuroaxonal Dystrophy
Late Infantile Neuroaxonal Dystrophy 		2 0 2 0.29 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		17 0 4 0.20 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 0.14 0 0
CUI: C0280214
Disease: stage, nasopharyngeal cancer
stage, nasopharyngeal cancer 		1 0 1 0.14 0 0
CUI: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 0.14 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 0.14 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 0.14 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 0.14 0 0
CUI: C1836522
Disease: Schindler Disease, Type II
Schindler Disease, Type II 		1 4 1 0.14 1 0.25
CUI: C1836525
Disease: White mater abnormalities in the posterior periventricular region
White mater abnormalities in the posterior periventricular region 		1 0 1 0.14 0 0
CUI: C1836544
Disease: Schindler Disease, Type I
Schindler Disease, Type I 		1 4 1 0.14 1 0.25
CUI: C1836545
Disease: Schindler Disease, Type III
Schindler Disease, Type III 		1 0 1 0.14 0 0
CUI: C1850363
Disease: Niemann-Pick Disease, Nova Scotian Type
Niemann-Pick Disease, Nova Scotian Type 		1 0 1 0.14 0 0
CUI: C1854182
Disease: PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) 		1 0 1 0.14 0 0
CUI: C1857747
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder) 		1 0 1 0.14 0 0
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 0 1 0.14 0 0
CUI: C2231324
Disease: Brucellosis, Pulmonary
Brucellosis, Pulmonary 		1 0 1 0.14 0 0
CUI: C2750220
Disease: Karak Syndrome
Karak Syndrome 		1 0 1 0.14 0 0
CUI: C3542549
Disease: SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE 		1 0 1 0.14 0 0
CUI: C4017105
Disease: NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM 		1 0 1 0.14 0 0
CUI: C4017106
Disease: NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM 		1 0 1 0.14 0 0
CUI: C4022743
Disease: T2 hypointense basal ganglia
T2 hypointense basal ganglia 		1 0 1 0.14 0 0
CUI: C4022768
Disease: Cerebellar gliosis
Cerebellar gliosis 		1 0 1 0.14 0 0