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: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 1.6E-02 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 1.6E-02 0 0
CUI: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 1.6E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 1.6E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 1.6E-02 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 1.6E-02 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 1.6E-02 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 1.6E-02 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 1.6E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 1.6E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 1.6E-02 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 1.6E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 1.6E-02 0 0
CUI: C0266429
Disease: Monorchism
Monorchism 		1 0 1 1.6E-02 0 0
CUI: C0268218
Disease: Maroteaux-Lamy syndrome, mild form
Maroteaux-Lamy syndrome, mild form 		1 0 1 1.6E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 1.6E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 1.6E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 1.6E-02 0 0
CUI: C0342841
Disease: Hunter's syndrome, severe form
Hunter's syndrome, severe form 		1 0 1 1.6E-02 0 0
CUI: C0342842
Disease: Hunter's syndrome, mild form
Hunter's syndrome, mild form 		1 0 1 1.6E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 1.6E-02 0 0
CUI: C0349661
Disease: Glial tumor of brain (disorder)
Glial tumor of brain (disorder) 		1 0 1 1.6E-02 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4 		1 0 1 1.6E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 1.6E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 1.6E-02 0 0