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: C0023600
Disease: Leydig cell hyperplasia
Leydig cell hyperplasia 		0 2 0 0 1 5.0E-02
CUI: C0266432
Disease: Leydig cell agenesis
Leydig cell agenesis 		0 21 0 0 1 2.6E-02
CUI: C0860158
Disease: Leydig Cell Hypoplasia
Leydig Cell Hypoplasia 		0 6 0 0 1 4.2E-02
CUI: C2674612
Disease: Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty
Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty 		0 1 0 0 1 5.3E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		210 0 1 2.1E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.3E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		145 0 1 2.4E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.4E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		135 0 1 2.4E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.5E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.5E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.5E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 0 1 2.5E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders 		121 0 1 2.5E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.5E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia 		118 0 1 2.5E-03 0 0
CUI: C0029231
Disease: Organic Mental Disorders, Substance-Induced
Organic Mental Disorders, Substance-Induced 		115 0 1 2.6E-03 0 0
CUI: C4316881
Disease: Prescription Drug Abuse
Prescription Drug Abuse 		115 0 1 2.6E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 2.6E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 2.6E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 2.6E-03 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 1 2.6E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 2.6E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 2.6E-03 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain 		103 0 1 2.6E-03 0 0