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: C3151343
Disease: SPINOCEREBELLAR ATAXIA 32
SPINOCEREBELLAR ATAXIA 32 		2 0 2 0.50 0 0
CUI: C0032586
Disease: Polyradiculopathy
Polyradiculopathy 		3 0 2 0.40 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia 		4 0 2 0.33 0 0
CUI: C1837728
Disease: AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder) 		4 0 2 0.33 0 0
CUI: C1848922
Disease: Hexosaminidase alpha-Subunit Deficiency (Variant B)
Hexosaminidase alpha-Subunit Deficiency (Variant B) 		4 0 2 0.33 0 0
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY 		4 0 2 0.33 0 0
CUI: C0282550
Disease: Persian Gulf Syndrome
Persian Gulf Syndrome 		5 0 2 0.29 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive 		5 0 2 0.29 0 0
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
Stereotyped behavior (Psychiatry) 		5 0 2 0.29 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 0.25 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch 		1 0 1 0.25 0 0
CUI: C1866053
Disease: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Congenital Heart Defects, and Posterior Embryotoxon 		1 0 1 0.25 0 0
CUI: C3809655
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R 		1 4 1 0.25 1 0.20
CUI: C4321359
Disease: Reduced insulin like growth factor binding protein acid labile subunit level
Reduced insulin like growth factor binding protein acid labile subunit level 		1 0 1 0.25 0 0
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		1 0 1 0.25 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 2 0.22 0 0
CUI: C0035066
Disease: Renal Artery Obstruction
Renal Artery Obstruction 		2 0 1 0.20 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 0.20 0 0
CUI: C1282365
Disease: Mixed type cataract
Mixed type cataract 		2 0 1 0.20 0 0
CUI: C1857761
Disease: Alagille Syndrome 2
Alagille Syndrome 2 		2 0 1 0.20 0 0
CUI: C1864570
Disease: Insulin insensitivity
Insulin insensitivity 		2 0 1 0.20 0 0
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		2 48 1 0.20 1 2.0E-02
CUI: C2930797
Disease: Hepatic ductular hypoplasia
Hepatic ductular hypoplasia 		2 0 1 0.20 0 0
CUI: C3715156
Disease: AMYOTROPHIC LATERAL SCLEROSIS 20
AMYOTROPHIC LATERAL SCLEROSIS 20 		2 0 1 0.20 0 0
CUI: C3805239
Disease: Mid aortic syndrome
Mid aortic syndrome 		2 0 1 0.20 0 0