Leber congenital amaurosis 5
Also known as: LCA5, LCA5 Leber congenital amaurosis, Leber congenital amaurosis 5, Leber congenital amaurosis caused by mutation in LCA5, Leber congenital amaurosis type 5, amaurosis congenita of Leber, type 5
Additional Disease Briefs
Leber congenital amaurosis 6
Also known as: LCA6, Leber congenital amaurosis 6, Leber congenital amaurosis caused by mutation in RPGRIP1, Leber congenital amaurosis type 6, RPGRIP1 Leber congenital amaurosis
Leber congenital amaurosis 7
Also known as: CRX Leber congenital amaurosis, LCA7, Leber congenital amaurosis 7, Leber congenital amaurosis caused by mutation in CRX, Leber congenital amaurosis type 7
Leber congenital amaurosis 8
Also known as: CRB1 Leber congenital amaurosis, LCA8, Leber congenital amaurosis 8, Leber congenital amaurosis caused by mutation in CRB1, Leber congenital amaurosis type 8
Leber congenital amaurosis 9
Also known as: LCA9, Leber congenital amaurosis 9, Leber congenital amaurosis caused by mutation in NMNAT1, Leber congenital amaurosis type 9, NMNAT1 Leber congenital amaurosis, amaurosis congenita of Leber, type 9
Leber congenital amaurosis with early-onset deafness
Also known as: LCAEOD, Leber congenital amaurosis with early-onset deafness
Leber optic atrophy and dystonia
Also known as: LDYT, LHON and dystonia, Leber Hereditary optic neuropathy with dystonia, Leber hereditary optic neuropathy with dystonia, Leber optic atrophy and dystonia, Leber's hereditary optic neuropathy with dystonia, Marsden syndrome, dystonia familial, with visual failure and striatal lucencies, dystonia, familial, with visual failure and striatal lucencies
Leber plus disease
Also known as: LHON plus disease
left superior vena cava persisting to left-sided atrium
Also known as: left SVC persisting to left-sided atrium, left superior caval vein persisting to left-sided atrium