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: C0599035
Disease: Hyperornithinemia
Hyperornithinemia 		3 65 3 0.38 2 2.4E-02
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 4 0.22 0 0
CUI: C1839531
Disease: Protein avoidance
Protein avoidance 		5 0 2 0.18 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 2 0.17 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 0.12 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 0.12 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 0.12 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 0.12 0 0
CUI: C0392180
Disease: Necrosis of placenta
Necrosis of placenta 		1 0 1 0.12 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 0.12 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 0.12 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 0.12 0 0
CUI: C1863080
Disease: ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF
ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF 		1 0 1 0.12 0 0
CUI: C1863081
Disease: alpha-Fetoprotein Deficiency
alpha-Fetoprotein Deficiency 		1 0 1 0.12 0 0
CUI: C2931728
Disease: Distal Trisomy 10q Syndrome
Distal Trisomy 10q Syndrome 		1 0 1 0.12 0 0
CUI: C3714958
Disease: PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C4017305
Disease: GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA
GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA 		1 0 1 0.12 0 0
CUI: C4021589
Disease: Absent glenoid fossa
Absent glenoid fossa 		1 0 1 0.12 0 0
CUI: C4022482
Disease: Chorioretinal hyperpigmentation
Chorioretinal hyperpigmentation 		1 0 1 0.12 0 0
CUI: C4022483
Disease: Chorioretinal hypopigmentation
Chorioretinal hypopigmentation 		1 0 1 0.12 0 0
CUI: C4073295
Disease: Decreased levels of alpha-fetoprotein
Decreased levels of alpha-fetoprotein 		1 0 1 0.12 0 0
CUI: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3 		1 0 1 0.12 0 0
CUI: C4225272
Disease: SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		1 0 1 0.12 0 0
CUI: C4330674
Disease: Metastatic Malignant Germ Cell Tumor
Metastatic Malignant Germ Cell Tumor 		1 0 1 0.12 0 0
CUI: C4552001
Disease: MEIER-GORLIN SYNDROME 1
MEIER-GORLIN SYNDROME 1 		1 0 1 0.12 0 0