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: C1838571
Disease: Ceroid Lipofuscinosis, Neuronal, 7
Ceroid Lipofuscinosis, Neuronal, 7 		3 0 2 0.33 0 0
CUI: C1838570
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 8
CEROID LIPOFUSCINOSIS, NEURONAL, 8 		5 43 2 0.25 2 4.7E-02
CUI: C1836852
Disease: Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material 		6 0 2 0.22 0 0
CUI: C1850442
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 5
CEROID LIPOFUSCINOSIS, NEURONAL, 5 		6 0 2 0.22 0 0
CUI: C4025728
Disease: Increased neuronal autofluorescent lipopigment
Increased neuronal autofluorescent lipopigment 		8 0 2 0.18 0 0
CUI: C0022797
Disease: Adult Neuronal Ceroid Lipofuscinosis
Adult Neuronal Ceroid Lipofuscinosis 		16 0 3 0.17 0 0
CUI: C1853507
Disease: Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations 		2 0 1 0.17 0 0
CUI: C1866282
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 6
CEROID LIPOFUSCINOSIS, NEURONAL, 6 		9 0 2 0.17 0 0
CUI: C4280575
Disease: Progressive brain disease
Progressive brain disease 		2 0 1 0.17 0 0
CUI: C0022340
Disease: Late-Infantile Neuronal Ceroid Lipfuscinosis
Late-Infantile Neuronal Ceroid Lipfuscinosis 		19 0 3 0.14 0 0
CUI: C0041952
Disease: Ureterolithiasis
Ureterolithiasis 		3 0 1 0.14 0 0
CUI: C1850447
Disease: Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
Rectilinear intracellular accumulation of autofluorescent lipopigment storage material 		3 0 1 0.14 0 0
CUI: C4021781
Disease: Abnormal nervous system electrophysiology
Abnormal nervous system electrophysiology 		3 0 1 0.14 0 0
CUI: C1836851
Disease: Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material 		5 0 1 0.11 0 0
CUI: C0751354
Disease: Myoclonus, Action
Myoclonus, Action 		6 0 1 1.0E-01 0 0
CUI: C1876161
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 2
CEROID LIPOFUSCINOSIS, NEURONAL, 2 		6 0 1 1.0E-01 0 0
CUI: C0751383
Disease: Juvenile Neuronal Ceroid Lipofuscinosis
Juvenile Neuronal Ceroid Lipofuscinosis 		52 0 4 7.5E-02 0 0
CUI: C0543874
Disease: Apraxia, oculomotor, Cogan type
Apraxia, oculomotor, Cogan type 		10 0 1 7.1E-02 0 0
CUI: C1847164
Disease: Morning myoclonic jerks
Morning myoclonic jerks 		11 0 1 6.7E-02 0 0
CUI: C1856565
Disease: Progressive psychomotor deterioration
Progressive psychomotor deterioration 		11 0 1 6.7E-02 0 0
CUI: C0334609
Disease: Hemangioblastic Meningioma
Hemangioblastic Meningioma 		12 0 1 6.2E-02 0 0
CUI: C0334610
Disease: Hemangiopericytic Meningioma
Hemangiopericytic Meningioma 		12 0 1 6.2E-02 0 0
CUI: C0457190
Disease: Xanthomatous Meningioma
Xanthomatous Meningioma 		12 0 1 6.2E-02 0 0
CUI: C0751303
Disease: Cerebral Convexity Meningioma
Cerebral Convexity Meningioma 		12 0 1 6.2E-02 0 0
CUI: C1334261
Disease: Intraorbital Meningioma
Intraorbital Meningioma 		12 0 1 6.2E-02 0 0