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: C1839564
Disease: Jensen syndrome
Jensen syndrome 		1 0 1 7.7E-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 7.7E-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 7.7E-02 0 0
CUI: C1847650
Disease: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES 		1 0 1 7.7E-02 0 0
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1 		1 0 1 7.7E-02 0 0
CUI: C1969957
Disease: Creutzfeldt-Jakob Disease, Heidenhain Variant
Creutzfeldt-Jakob Disease, Heidenhain Variant 		1 0 1 7.7E-02 0 0
CUI: C1997740
Disease: Segmental dystonia
Segmental dystonia 		15 0 2 7.7E-02 0 0
CUI: C2316460
Disease: Pseudobulbar affect
Pseudobulbar affect 		1 0 1 7.7E-02 0 0
CUI: C2363747
Disease: Neurological decompensation
Neurological decompensation 		1 0 1 7.7E-02 0 0
CUI: C2676244
Disease: Leukodystrophy, Hypomyelinating, 6
Leukodystrophy, Hypomyelinating, 6 		1 28 1 7.7E-02 1 2.9E-02
CUI: C2751506
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL 		1 0 1 7.7E-02 0 0
CUI: C2931022
Disease: Amyloidosis, Cerebral, with Spongiform Encephalopathy
Amyloidosis, Cerebral, with Spongiform Encephalopathy 		1 0 1 7.7E-02 0 0
CUI: C2931859
Disease: Acquired CJD
Acquired CJD 		1 0 1 7.7E-02 0 0
CUI: C3151038
Disease: ACNE INVERSA, FAMILIAL, 3
ACNE INVERSA, FAMILIAL, 3 		1 0 1 7.7E-02 0 0
CUI: C3160720
Disease: Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1u 		1 0 1 7.7E-02 0 0
CUI: C3267131
Disease: Psychogenic movement disorder
Psychogenic movement disorder 		1 0 1 7.7E-02 0 0
CUI: C3553788
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 		1 38 1 7.7E-02 1 2.3E-02
CUI: C3710741
Disease: Torticollis, familial
Torticollis, familial 		1 0 1 7.7E-02 0 0
CUI: C3805618
Disease: CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED 		1 0 1 7.7E-02 0 0
CUI: C4015780
Disease: ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES
ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES 		1 0 1 7.7E-02 0 0
CUI: C4015781
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES 		1 0 1 7.7E-02 0 0
CUI: C4015782
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS 		1 1 1 7.7E-02 1 0.14
CUI: C4016920
Disease: DYSTONIA 1, TORSION, LATE-ONSET
DYSTONIA 1, TORSION, LATE-ONSET 		1 0 1 7.7E-02 0 0
CUI: C4021229
Disease: Low insertion of columella
Low insertion of columella 		1 0 1 7.7E-02 0 0
CUI: C4022162
Disease: Amyloidosis of peripheral nerves
Amyloidosis of peripheral nerves 		1 0 1 7.7E-02 0 0