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: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 4.2E-04
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 4.2E-04
CUI: C4016689
Disease: PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO
PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO 		0 1 0 0 1 4.2E-04
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 3.6E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 3.6E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 3.6E-04 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 1 3.6E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 3.6E-04 0 0
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		39 0 1 3.6E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 0 1 3.6E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 1 3.6E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 3.6E-04 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy 		32 0 1 3.6E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination 		32 0 1 3.6E-04 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 1 3.6E-04 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 1 3.6E-04 0 0
CUI: C1855333
Disease: External genital hypoplasia
External genital hypoplasia 		29 0 1 3.6E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 1 3.6E-04 0 0
CUI: C4551568
Disease: Joubert syndrome 1
Joubert syndrome 1 		26 0 1 3.6E-04 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 1 3.6E-04 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 1 3.6E-04 0 0
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		24 0 1 3.6E-04 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		24 0 1 3.6E-04 0 0
CUI: C0233849
Disease: Personality Traits
Personality Traits 		24 0 1 3.6E-04 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy 		24 0 1 3.6E-04 0 0