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: C0268543
Disease: Hyperammonemia, type III
Hyperammonemia, type III 		1 0 1 4.8E-03 0 0
CUI: C0270075
Disease: Perinatal disorder
Perinatal disorder 		1 0 1 4.8E-03 0 0
CUI: C0270224
Disease: Tetany, Neonatal
Tetany, Neonatal 		1 0 1 4.8E-03 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 4.8E-03 0 0
CUI: C0275616
Disease: Infection due to Clostridium chauvoei
Infection due to Clostridium chauvoei 		1 0 1 4.8E-03 0 0
CUI: C0279697
Disease: salivary gland squamous cell carcinoma
salivary gland squamous cell carcinoma 		1 0 1 4.8E-03 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 4.8E-03 0 0
CUI: C0334338
Disease: Endometrioid adenoma, borderline malignancy
Endometrioid adenoma, borderline malignancy 		1 0 1 4.8E-03 0 0
CUI: C0334566
Disease: Ghost Cell Odontogenic Carcinoma
Ghost Cell Odontogenic Carcinoma 		1 0 1 4.8E-03 0 0
CUI: C0340007
Disease: Catamenial pneumothorax
Catamenial pneumothorax 		1 0 1 4.8E-03 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 4.8E-03 0 0
CUI: C0406571
Disease: Superficial fibromatosis
Superficial fibromatosis 		1 0 1 4.8E-03 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 4.8E-03 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 4.8E-03 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 4.8E-03 0 0
CUI: C0477972
Disease: Other specified congenital malformations of brain
Other specified congenital malformations of brain 		1 0 1 4.8E-03 0 0
CUI: C0494423
Disease: Specific developmental disorders of speech and language
Specific developmental disorders of speech and language 		1 0 1 4.8E-03 0 0
CUI: C0549651
Disease: Abnormality of the lens
Abnormality of the lens 		1 0 1 4.8E-03 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 4.8E-03 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 4.8E-03 0 0
CUI: C0701826
Disease: Perinatal death
Perinatal death 		1 0 1 4.8E-03 0 0
CUI: C0745745
Disease: liver disease parenchymal
liver disease parenchymal 		1 0 1 4.8E-03 0 0
CUI: C0751050
Disease: Communication Disorders, Developmental
Communication Disorders, Developmental 		1 0 1 4.8E-03 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 4.8E-03 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 4.8E-03 0 0