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: C4023376
Disease: Abnormality of the dorsal column of the spinal cord
Abnormality of the dorsal column of the spinal cord 		2 0 2 0.20 0 0
CUI: C0231698
Disease: Gait, Scissors
Gait, Scissors 		12 0 2 1.0E-01 0 0
CUI: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 1.0E-01 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 1.0E-01 0 0
CUI: C0497219
Disease: Hearing complaints (excluding H84-86)
Hearing complaints (excluding H84-86) 		1 0 1 1.0E-01 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 1.0E-01 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 1.0E-01 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 1.0E-01 0 0
CUI: C3151038
Disease: ACNE INVERSA, FAMILIAL, 3
ACNE INVERSA, FAMILIAL, 3 		1 0 1 1.0E-01 0 0
CUI: C3160720
Disease: Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1u 		1 0 1 1.0E-01 0 0
CUI: C3553331
Disease: Subcortical heterotopia
Subcortical heterotopia 		1 0 1 1.0E-01 0 0
CUI: C3554168
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14 		1 0 1 1.0E-01 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 1.0E-01 0 0
CUI: C4015781
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES 		1 0 1 1.0E-01 0 0
CUI: C4015782
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS 		1 1 1 1.0E-01 1 0.33
CUI: C4017059
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED
CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED 		1 0 1 1.0E-01 0 0
CUI: C4022166
Disease: EMG: myokymic discharges
EMG: myokymic discharges 		1 0 1 1.0E-01 0 0
CUI: C4022899
Disease: Bilateral wrist flexion contracture
Bilateral wrist flexion contracture 		1 1 1 1.0E-01 1 0.33
CUI: C4023352
Disease: Abnormality of higher mental function
Abnormality of higher mental function 		1 0 1 1.0E-01 0 0
CUI: C4024607
Disease: Exercise-induced leg cramps
Exercise-induced leg cramps 		1 0 1 1.0E-01 0 0
CUI: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3 		1 0 1 1.0E-01 0 0
CUI: C4225272
Disease: SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C4285793
Disease: Paroxysmal sympathetic hyperactivity
Paroxysmal sympathetic hyperactivity 		1 0 1 1.0E-01 0 0
CUI: C4310750
Disease: SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C4310765
Disease: Hypermanganesemia with dystonia 2
Hypermanganesemia with dystonia 2 		1 0 1 1.0E-01 0 0