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: C1970180
Disease: Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation 		4 0 3 0.30 0 0
CUI: C1969084
Disease: Pontocerebellar Hypoplasia Type 6
Pontocerebellar Hypoplasia Type 6 		5 0 3 0.27 0 0
CUI: C3809008
Disease: HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY
HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY 		2 0 2 0.22 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder 		10 0 2 0.12 0 0
CUI: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness 		10 0 2 0.12 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 0.11 0 0
CUI: C0599949
Disease: Arterial Stiffness
Arterial Stiffness 		1 0 1 0.11 0 0
CUI: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 0.11 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 0.11 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 0.11 0 0
CUI: C1280768
Disease: Axenfeld syndrome
Axenfeld syndrome 		1 0 1 0.11 0 0
CUI: C1843512
Disease: BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE 		1 0 1 0.11 0 0
CUI: C1854182
Disease: PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) 		1 0 1 0.11 0 0
CUI: C1867327
Disease: RETINAL ARTERIES, TORTUOSITY OF
RETINAL ARTERIES, TORTUOSITY OF 		1 0 1 0.11 0 0
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 0 1 0.11 0 0
CUI: C2675650
Disease: Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly 		1 0 1 0.11 0 0
CUI: C2930808
Disease: Familial vascular leukoencephalopathy
Familial vascular leukoencephalopathy 		1 0 1 0.11 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 0.11 0 0
CUI: C3496177
Disease: Atypical psychosis
Atypical psychosis 		1 0 1 0.11 0 0
CUI: C4013035
Disease: BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES
BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES 		1 0 1 0.11 0 0
CUI: C4015323
Disease: LEUKODYSTROPHY, HYPOMYELINATING, 9
LEUKODYSTROPHY, HYPOMYELINATING, 9 		1 0 1 0.11 0 0
CUI: C4746984
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12 		1 0 1 0.11 0 0
CUI: C4755254
Disease: Hypomyelination with brain stem and spinal cord involvement and leg spasticity
Hypomyelination with brain stem and spinal cord involvement and leg spasticity 		1 0 1 0.11 0 0
CUI: C0221011
Disease: Malignant Atrophic Papulosis
Malignant Atrophic Papulosis 		2 0 1 1.0E-01 0 0
CUI: C0270173
Disease: TORCH syndrome
TORCH syndrome 		2 0 1 1.0E-01 0 0