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: C0751664
Disease: Canavan Disease, Neonatal
Canavan Disease, Neonatal 		1 0 1 1.00 0 0
CUI: C0751665
Disease: Canavan Disease, Sporadic Form
Canavan Disease, Sporadic Form 		1 0 1 1.00 0 0
CUI: C0751666
Disease: Canavan Disease, Infantile
Canavan Disease, Infantile 		1 0 1 1.00 0 0
CUI: C0751667
Disease: Canavan Disease, Juvenile
Canavan Disease, Juvenile 		1 0 1 1.00 0 0
CUI: C0751663
Disease: Canavan Disease, Familial Form
Canavan Disease, Familial Form 		2 0 1 0.50 0 0
CUI: C4017127
Disease: CANAVAN DISEASE, MILD
CANAVAN DISEASE, MILD 		2 0 1 0.50 0 0
CUI: C4025665
Disease: Aplasia/Hypoplasia involving the central nervous system
Aplasia/Hypoplasia involving the central nervous system 		2 0 1 0.50 0 0
CUI: C0009730
Disease: Spinal meningocele
Spinal meningocele 		10 0 1 1.0E-01 0 0
CUI: C0270707
Disease: Kluver-Bucy Syndrome
Kluver-Bucy Syndrome 		10 0 1 1.0E-01 0 0
CUI: C1879828
Disease: Benign Teratoma
Benign Teratoma 		10 0 1 1.0E-01 0 0
CUI: C0025299
Disease: Meningocele
Meningocele 		11 0 1 9.1E-02 0 0
CUI: C0206307
Disease: Canavan Disease
Canavan Disease 		12 0 1 8.3E-02 0 0
CUI: C0154671
Disease: Degenerative brain disorder
Degenerative brain disorder 		16 0 1 6.2E-02 0 0
CUI: C0281658
Disease: Intraocular Lymphoma
Intraocular Lymphoma 		19 0 1 5.3E-02 0 0
CUI: C3840083
Disease: Late closure of anterior fontanel
Late closure of anterior fontanel 		21 0 1 4.8E-02 0 0
CUI: C3532239
Disease: Mitochondrial cardiomyopathy
Mitochondrial cardiomyopathy 		23 0 1 4.3E-02 0 0
CUI: C0039373
Disease: Tay-Sachs Disease
Tay-Sachs Disease 		26 0 1 3.8E-02 0 0
CUI: C0151818
Disease: Opisthotonus
Opisthotonus 		32 0 1 3.1E-02 0 0
CUI: C0011649
Disease: Dermoid Cyst
Dermoid Cyst 		33 0 1 3.0E-02 0 0
CUI: C1261470
Disease: Congenital meningocele
Congenital meningocele 		33 0 1 3.0E-02 0 0
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		36 0 1 2.8E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 2.7E-02 0 0
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		39 0 1 2.6E-02 0 0
CUI: C0233523
Disease: Antisocial behavior
Antisocial behavior 		51 0 1 2.0E-02 0 0
CUI: C0338474
Disease: Central nervous system demyelination
Central nervous system demyelination 		52 0 1 1.9E-02 0 0