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: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 1.6E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 1.8E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 1.9E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 1.9E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 1.9E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 1.9E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 1 1.9E-03 0 0
CUI: C1835884
Disease: Triangular face
Triangular face 		111 0 1 2.0E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 2.0E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 2.0E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 2.0E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling 		95 0 1 2.0E-03 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		95 0 1 2.0E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 1 2.0E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 1 2.0E-03 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		86 0 1 2.1E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 2.1E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 2.1E-03 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 1 2.1E-03 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		80 0 1 2.1E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 2.1E-03 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 1 2.1E-03 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 1 2.1E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 2.1E-03 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		70 0 1 2.1E-03 0 0