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: C0000729
Disease: Abdominal Cramps
Abdominal Cramps 		1 0 1 8.3E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 8.3E-03 0 0
CUI: C0004048
Disease: Inspiration function
Inspiration function 		1 0 1 8.3E-03 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 8.3E-03 0 0
CUI: C0009769
Disease: Conjunctivitis, Giant Papillary
Conjunctivitis, Giant Papillary 		1 0 1 8.3E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 8.3E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 8.3E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 8.3E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 8.3E-03 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 8.3E-03 0 0
CUI: C0035468
Disease: Rhinoscleroma
Rhinoscleroma 		1 0 1 8.3E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 8.3E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 8.3E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 8.3E-03 1 7.7E-02
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 8.3E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 8.3E-03 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex 		1 0 1 8.3E-03 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive 		1 0 1 8.3E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 8.3E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 8.3E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 8.3E-03 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 8.3E-03 0 0
CUI: C0265257
Disease: Genee-Wiedemann syndrome
Genee-Wiedemann syndrome 		1 0 1 8.3E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 8.3E-03 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 8.3E-03 1 9.1E-02