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: C0158371
Disease: Acute osteomyelitis
Acute osteomyelitis 		2 0 1 5.6E-02 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 0 1 5.6E-02 0 0
CUI: C0995195
Disease: Anoxia of brain
Anoxia of brain 		2 0 1 5.6E-02 0 0
CUI: C1140716
Disease: Hypoxic Brain Damage
Hypoxic Brain Damage 		2 0 1 5.6E-02 0 0
CUI: C4024632
Disease: Gonadal dysgenesis with female appearance, male
Gonadal dysgenesis with female appearance, male 		2 0 1 5.6E-02 0 0
CUI: C4039867
Disease: Acute hypoxemic respiratory failure
Acute hypoxemic respiratory failure 		2 0 1 5.6E-02 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 1 5.6E-02 0 0
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement 		2 0 1 5.6E-02 0 0
CUI: C0036347
Disease: Schizophrenia, Disorganized
Schizophrenia, Disorganized 		3 0 1 5.3E-02 0 0
CUI: C0266335
Disease: Congenital anomaly of the bladder
Congenital anomaly of the bladder 		3 0 1 5.3E-02 0 0
CUI: C0429702
Disease: Respiratory quotient
Respiratory quotient 		3 0 1 5.3E-02 0 0
CUI: C2919194
Disease: Sporadic olivopontocerebellar atrophy
Sporadic olivopontocerebellar atrophy 		3 0 1 5.3E-02 0 0
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13 		3 0 1 5.3E-02 0 0
CUI: C3665905
Disease: Passenger lymphocyte syndrome
Passenger lymphocyte syndrome 		3 0 1 5.3E-02 0 0
CUI: C3714744
Disease: Psychosexual dysfunction
Psychosexual dysfunction 		3 0 1 5.3E-02 0 0
CUI: C4476760
Disease: Visual fixation instability
Visual fixation instability 		3 0 1 5.3E-02 0 0
CUI: C4699189
Disease: Nonprogressive/congenital
Nonprogressive/congenital 		3 0 1 5.3E-02 0 0
CUI: C4706387
Disease: Acute necrotizing encephalopathy of childhood
Acute necrotizing encephalopathy of childhood 		3 0 1 5.3E-02 0 0
CUI: C4025860
Disease: Hearing abnormality
Hearing abnormality 		24 0 2 5.1E-02 0 0
CUI: C0023439
Disease: Leukemia, Eosinophilic, Acute
Leukemia, Eosinophilic, Acute 		4 0 1 5.0E-02 0 0
CUI: C0026961
Disease: Mydriasis
Mydriasis 		25 0 2 5.0E-02 0 0
CUI: C0235575
Disease: Hemolytic reaction
Hemolytic reaction 		4 0 1 5.0E-02 0 0
CUI: C0344542
Disease: Aniridia type 1
Aniridia type 1 		4 0 1 5.0E-02 0 0
CUI: C0431401
Disease: Gillespie syndrome
Gillespie syndrome 		4 0 1 5.0E-02 0 0
CUI: C1333003
Disease: Childhood Kidney Neoplasm
Childhood Kidney Neoplasm 		4 0 1 5.0E-02 0 0