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: 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
Hearing complaints (excluding H84-86)
1 0 1 1.0E-01 0 0
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
1 0 1 1.0E-01 0 0
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
1 0 1 1.0E-01 0 0
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
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14
1 0 1 1.0E-01 0 0
ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES
1 0 1 1.0E-01 0 0
ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
1 0 1 1.0E-01 0 0
ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
1 1 1 1.0E-01 1 0.33
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
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
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
1 0 1 1.0E-01 0 0
Paroxysmal sympathetic hyperactivity
1 0 1 1.0E-01 0 0
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
CUI: C4693824
Disease: VERVERI-BRADY SYNDROME
VERVERI-BRADY SYNDROME
1 5 1 1.0E-01 1 0.14
CUI: C4703584
Disease: Optic ataxia
Optic ataxia
1 0 1 1.0E-01 0 0