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: C4023728
Disease: 1-5 finger syndactyly
1-5 finger syndactyly 		3 0 1 5.0E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		55 0 1 1.4E-02 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals 		3 0 1 5.0E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 2 6.3E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 121 6 6.5E-03 1 8.3E-03
CUI: C4025711
Disease: Abnormal caudate nucleus morphology
Abnormal caudate nucleus morphology 		9 0 1 3.8E-02 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 1.9E-02 0 0
CUI: C4022922
Disease: Abnormal enzyme/coenzyme activity
Abnormal enzyme/coenzyme activity 		13 0 1 3.3E-02 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 3 0.11 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 1 3.3E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 7.6E-03 0 0
CUI: C2674737
Disease: Abnormality of finger
Abnormality of finger 		8 0 1 4.0E-02 0 0
CUI: C4082761
Disease: Abnormality of limb bone morphology
Abnormality of limb bone morphology 		3 0 1 5.0E-02 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 1 5.3E-03 0 0
CUI: C1832160
Disease: Abnormality of temperature regulation
Abnormality of temperature regulation 		19 0 1 2.8E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 1.1E-02 0 0
CUI: C2673431
Disease: Abnormality of the periventricular white matter
Abnormality of the periventricular white matter 		45 0 1 1.6E-02 0 0
CUI: C4025397
Disease: Abnormality of the scaphoid
Abnormality of the scaphoid 		2 0 1 5.3E-02 0 0
CUI: C4025390
Disease: Abnormality of the trapezium
Abnormality of the trapezium 		2 0 1 5.3E-02 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 6.9E-03 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 1 3.2E-02 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 1 9.4E-03 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 3 2.4E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 3 1.4E-02 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 4.0E-03 0 0