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: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 7.2E-03 0 0
CUI: C0012767
Disease: Tooth eruption disorder
Tooth eruption disorder 		1 0 1 7.2E-03 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced 		1 0 1 7.2E-03 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 7.2E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 7.2E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 7.2E-03 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 7.2E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 7.2E-03 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 7.2E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 7.2E-03 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 7.2E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 7.2E-03 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis 		1 0 1 7.2E-03 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 7.2E-03 0 0
CUI: C0151686
Disease: Growth retardation
Growth retardation 		1 0 1 7.2E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 7.2E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 7.2E-03 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 7.2E-03 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 7.2E-03 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 7.2E-03 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast 		1 0 1 7.2E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 7.2E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 7.2E-03 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 7.2E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 7.2E-03 0 0