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: C4280806
Disease: Calcium oxalate kidney stones
Calcium oxalate kidney stones 		4 0 1 0.12 0 0
CUI: C0085132
Disease: Mucopolysaccharidosis VII
Mucopolysaccharidosis VII 		5 0 1 0.11 0 0
CUI: C0524812
Disease: Intracranial Hypotension
Intracranial Hypotension 		5 0 1 0.11 0 0
CUI: C1866772
Disease: Abnormal nerve conduction velocity
Abnormal nerve conduction velocity 		5 0 1 0.11 0 0
CUI: C0009918
Disease: Contracture of joint
Contracture of joint 		36 0 4 0.11 0 0
CUI: C2718068
Disease: beta-Galactosidase Deficiency
beta-Galactosidase Deficiency 		6 0 1 1.0E-01 0 0
CUI: C0302180
Disease: Condyloma
Condyloma 		40 0 4 9.8E-02 0 0
CUI: C1848103
Disease: Narrow pelvis bone
Narrow pelvis bone 		8 0 1 8.3E-02 0 0
CUI: C4023009
Disease: Constrictive median neuropathy
Constrictive median neuropathy 		8 0 1 8.3E-02 0 0
CUI: C4024726
Disease: Mucopolysacchariduria
Mucopolysacchariduria 		8 0 1 8.3E-02 0 0
CUI: C0026703
Disease: Mucopolysaccharidoses
Mucopolysaccharidoses 		48 0 4 8.2E-02 0 0
CUI: C1298681
Disease: Oxalosis
Oxalosis 		9 0 1 7.7E-02 0 0
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination 		9 0 1 7.7E-02 0 0
CUI: C0265673
Disease: Congenital kyphosis
Congenital kyphosis 		54 0 4 7.3E-02 0 0
CUI: C1854718
Disease: J-shaped sella turcica
J-shaped sella turcica 		10 0 1 7.1E-02 0 0
CUI: C1863351
Disease: Calvarial hyperostosis
Calvarial hyperostosis 		10 0 1 7.1E-02 0 0
CUI: C0014117
Disease: Endocardial Fibroelastosis
Endocardial Fibroelastosis 		11 0 1 6.7E-02 0 0
CUI: C0015929
Disease: Fetal Diseases
Fetal Diseases 		11 0 1 6.7E-02 0 0
CUI: C0342643
Disease: Autosomal recessive hypophosphatemic vitamin D refractory rickets
Autosomal recessive hypophosphatemic vitamin D refractory rickets 		11 2 1 6.7E-02 1 4.8E-02
CUI: C0743360
Disease: Recurrent ear infections
Recurrent ear infections 		11 0 1 6.7E-02 0 0
CUI: C2748652
Disease: Large face
Large face 		11 0 1 6.7E-02 0 0
CUI: C3494976
Disease: Migrating partial seizures in infancy
Migrating partial seizures in infancy 		11 2 1 6.7E-02 1 4.8E-02
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology 		11 0 1 6.7E-02 0 0
CUI: C0037926
Disease: Compression of spinal cord
Compression of spinal cord 		60 0 4 6.6E-02 0 0
CUI: C4021386
Disease: Abnormality of the elbow
Abnormality of the elbow 		12 0 1 6.2E-02 0 0