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: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 2.6E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 2.6E-02 0 0
CUI: C0155379
Disease: Nystagmus associated with disorder of the vestibular system
Nystagmus associated with disorder of the vestibular system 		1 0 1 2.6E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 2.6E-02 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 2.6E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 2.6E-02 0 0
CUI: C0393577
Disease: Pallidal degeneration
Pallidal degeneration 		1 0 1 2.6E-02 0 0
CUI: C0751878
Disease: Vasculitis, Central Nervous System
Vasculitis, Central Nervous System 		1 0 1 2.6E-02 0 0
CUI: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 2.6E-02 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 2.6E-02 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 2.6E-02 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 2.6E-02 0 0
CUI: C0919678
Disease: Protein S measurement
Protein S measurement 		1 0 1 2.6E-02 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 2.6E-02 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 2.6E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.6E-02 0 0
CUI: C1836076
Disease: Amyotrophic Lateral Sclerosis, Chmp2B-Related
Amyotrophic Lateral Sclerosis, Chmp2B-Related 		1 0 1 2.6E-02 0 0
CUI: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 2.6E-02 0 0
CUI: C1842197
Disease: Charcot-Marie-Tooth Disease, Recessive Intermediate A
Charcot-Marie-Tooth Disease, Recessive Intermediate A 		1 0 1 2.6E-02 0 0
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		1 0 1 2.6E-02 0 0
CUI: C1843014
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques 		1 0 1 2.6E-02 0 0
CUI: C1843015
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia 		1 0 1 2.6E-02 0 0
CUI: C1843315
Disease: Neuronopathy, Distal Hereditary Motor, Type Viib
Neuronopathy, Distal Hereditary Motor, Type Viib 		1 0 1 2.6E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 2.6E-02 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 2.6E-02 0 0