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: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 1 3.2E-04 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc 		26 0 1 3.2E-04 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		25 0 1 3.2E-04 0 0
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		24 42 1 3.2E-04 1 2.5E-03
CUI: C4021728
Disease: EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation 		24 0 1 3.2E-04 0 0
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		23 0 1 3.2E-04 0 0
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment 		22 0 1 3.2E-04 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 1 3.2E-04 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		21 0 1 3.2E-04 0 0
CUI: C1834536
Disease: Weakness of the intrinsic hand muscles
Weakness of the intrinsic hand muscles 		21 0 1 3.2E-04 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 1 3.2E-04 0 0
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		21 0 1 3.2E-04 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 1 3.2E-04 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		20 0 1 3.2E-04 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 1 3.2E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 3.2E-04 0 0
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 0 1 3.2E-04 0 0
CUI: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 3.2E-04 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 1 3.2E-04 0 0
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality 		18 0 1 3.2E-04 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 1 3.2E-04 0 0
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		17 0 1 3.2E-04 0 0
CUI: C0344424
Disease: Ventricular Arrhythmia by ECG Finding
Ventricular Arrhythmia by ECG Finding 		17 0 1 3.2E-04 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 1 3.2E-04 0 0
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy 		17 0 1 3.2E-04 0 0