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: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 6.7E-02 0 0
CUI: C0860602
Disease: Anxious personality
Anxious personality 		1 0 1 6.7E-02 0 0
CUI: C1561993
Disease: Valvular sclerosis
Valvular sclerosis 		1 0 1 6.7E-02 0 0
CUI: C1834383
Disease: Thickening of the lateral border of the scapula
Thickening of the lateral border of the scapula 		1 0 1 6.7E-02 0 0
CUI: C1834392
Disease: Disproportionate prominence of the femoral medial condyle
Disproportionate prominence of the femoral medial condyle 		1 0 1 6.7E-02 0 0
CUI: C1868158
Disease: Absence of pectoralis minor muscle
Absence of pectoralis minor muscle 		1 0 1 6.7E-02 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 6.7E-02 0 0
CUI: C2677325
Disease: RETINITIS PIGMENTOSA 29 (disorder)
RETINITIS PIGMENTOSA 29 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C3554018
Disease: SINOATRIAL NODE DYSFUNCTION AND DEAFNESS
SINOATRIAL NODE DYSFUNCTION AND DEAFNESS 		1 0 1 6.7E-02 0 0
CUI: C3805764
Disease: Biceps aplasia
Biceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C3805765
Disease: Quadriceps aplasia
Quadriceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C3809609
Disease: PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES
PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C3810484
Disease: Triceps aplasia
Triceps aplasia 		1 0 1 6.7E-02 0 0
CUI: C4014833
Disease: IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C4016698
Disease: IMMUNODEFICIENCY 26 WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C4024210
Disease: Lester's sign
Lester's sign 		1 0 1 6.7E-02 0 0
CUI: C4024693
Disease: Factor X activation deficiency
Factor X activation deficiency 		1 0 1 6.7E-02 0 0
CUI: C4025048
Disease: Elongated radius
Elongated radius 		1 0 1 6.7E-02 0 0
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		1 0 1 6.7E-02 0 0
CUI: C0001364
Disease: Massive Hepatic Necrosis
Massive Hepatic Necrosis 		2 0 1 6.2E-02 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		2 0 1 6.2E-02 0 0
CUI: C1834384
Disease: Glenoid fossa hypoplasia
Glenoid fossa hypoplasia 		2 0 1 6.2E-02 0 0
CUI: C1862391
Disease: ASD I
ASD I 		2 0 1 6.2E-02 0 0
CUI: C1862392
Disease: Atrial Septal Defect, Secundum Type
Atrial Septal Defect, Secundum Type 		2 0 1 6.2E-02 0 0
CUI: C1862393
Disease: ASD II
ASD II 		2 0 1 6.2E-02 0 0