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: C0221773
Disease: Hyperamylasemia
Hyperamylasemia 		14 0 3 7.9E-02 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		29 0 4 7.7E-02 0 0
CUI: C0041972
Disease: Urethral Obstruction
Urethral Obstruction 		16 0 3 7.5E-02 0 0
CUI: C0349231
Disease: Phobic anxiety disorder
Phobic anxiety disorder 		31 0 4 7.4E-02 0 0
CUI: C4022392
Disease: Early onset of sexual maturation
Early onset of sexual maturation 		2 0 2 7.4E-02 0 0
CUI: C4531100
Disease: Negative affectivity
Negative affectivity 		17 0 3 7.3E-02 0 0
CUI: C0520887
Disease: ST segment depression (finding)
ST segment depression (finding) 		3 0 2 7.1E-02 0 0
CUI: C0521991
Disease: Symptoms of stress
Symptoms of stress 		33 0 4 7.1E-02 0 0
CUI: C1969408
Disease: Prominent U wave
Prominent U wave 		3 0 2 7.1E-02 0 0
CUI: C2828000
Disease: X-Linked Inherited Disorder
X-Linked Inherited Disorder 		3 0 2 7.1E-02 0 0
CUI: C0271728
Disease: Secondary hyperaldosteronism
Secondary hyperaldosteronism 		4 0 2 6.9E-02 0 0
CUI: C1866500
Disease: Low-to-normal blood pressure
Low-to-normal blood pressure 		4 0 2 6.9E-02 0 0
CUI: C3888890
Disease: Polyuria-polydipsia syndrome
Polyuria-polydipsia syndrome 		4 0 2 6.9E-02 0 0
CUI: C0865424
Disease: Adult attention deficit hyperactivity disorder
Adult attention deficit hyperactivity disorder 		20 0 3 6.8E-02 0 0
CUI: C0039494
Disease: Temporomandibular Joint Disorders
Temporomandibular Joint Disorders 		84 0 7 6.7E-02 0 0
CUI: C0020450
Disease: Hyperemesis Gravidarum
Hyperemesis Gravidarum 		21 0 3 6.7E-02 0 0
CUI: C0149779
Disease: Somatization
Somatization 		21 0 3 6.7E-02 0 0
CUI: C0403555
Disease: Ochoa syndrome
Ochoa syndrome 		5 0 2 6.7E-02 0 0
CUI: C0600125
Disease: Prolonged PR interval
Prolonged PR interval 		5 0 2 6.7E-02 0 0
CUI: C0857122
Disease: Hyponatraemic
Hyponatraemic 		5 0 2 6.7E-02 0 0
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		5 0 2 6.7E-02 0 0
CUI: C4331824
Disease: Autosomal Dominant Neurohypophyseal Diabetes Insipidus
Autosomal Dominant Neurohypophyseal Diabetes Insipidus 		5 0 2 6.7E-02 0 0
CUI: C4552839
Disease: Hypomagnesemia, CTCAE
Hypomagnesemia, CTCAE 		21 0 3 6.7E-02 0 0
CUI: C0025048
Disease: Meconium Aspiration Syndrome
Meconium Aspiration Syndrome 		38 0 4 6.6E-02 0 0
CUI: C0268024
Disease: Hyperkalemia, diminished renal excretion
Hyperkalemia, diminished renal excretion 		6 0 2 6.5E-02 0 0