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: C4225326
Disease: FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3 		2 20 2 1.00 4 0.16
CUI: C4310693
Disease: NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET
NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET 		1 0 1 0.50 0 0
CUI: C0339652
Disease: Vertical gaze palsy
Vertical gaze palsy 		2 0 1 0.33 0 0
CUI: C2931290
Disease: Welander distal myopathy, Swedish type
Welander distal myopathy, Swedish type 		2 0 1 0.33 0 0
CUI: C4085251
Disease: PAGET DISEASE OF BONE 2, EARLY-ONSET
PAGET DISEASE OF BONE 2, EARLY-ONSET 		2 4 1 0.33 1 8.3E-02
CUI: C1855845
Disease: Patchy osteosclerosis
Patchy osteosclerosis 		3 0 1 0.25 0 0
CUI: C2931732
Disease: Familial Paget's disease of bone
Familial Paget's disease of bone 		3 0 1 0.25 0 0
CUI: C0432292
Disease: Familial expansile osteolysis
Familial expansile osteolysis 		5 0 1 0.17 0 0
CUI: C1333294
Disease: ALK positive large B-cell lymphoma
ALK positive large B-cell lymphoma 		5 0 1 0.17 0 0
CUI: C0037944
Disease: Spinal Stenosis
Spinal Stenosis 		6 0 1 0.14 0 0
CUI: C0240231
Disease: Fractures of the long bones
Fractures of the long bones 		6 0 1 0.14 0 0
CUI: C0221054
Disease: Welander Distal Myopathy
Welander Distal Myopathy 		8 0 1 0.11 0 0
CUI: C1707544
Disease: Cutaneous Fibrous Histiocytoma, Epithelioid Variant
Cutaneous Fibrous Histiocytoma, Epithelioid Variant 		8 0 1 0.11 0 0
CUI: C1849485
Disease: Neuronal loss in the cerebral cortex
Neuronal loss in the cerebral cortex 		8 0 1 0.11 0 0
CUI: C0919974
Disease: Abulia
Abulia 		9 0 1 1.0E-01 0 0
CUI: C1509147
Disease: Histiocytoma
Histiocytoma 		10 0 1 9.1E-02 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality 		10 0 1 9.1E-02 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity 		10 0 1 9.1E-02 0 0
CUI: C1843477
Disease: Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex Superficialis 		11 0 1 8.3E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy 		11 0 1 8.3E-02 0 0
CUI: C1863843
Disease: Neuronal intranuclear inclusion disease
Neuronal intranuclear inclusion disease 		12 0 1 7.7E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 4 1 7.1E-02 1 8.3E-02
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 1 7.1E-02 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		13 0 1 7.1E-02 0 0
CUI: C0206631
Disease: Lipomatous neoplasm
Lipomatous neoplasm 		14 0 1 6.7E-02 0 0