Kosmix
One sec... we're building your guide for
Leber Congenital Amaurosis
Leber congenital amaurosis
Overview
Anatomy
Health Providers & Organizations
Main ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Ophthalmology
(26)
Retinopathy
Retinitis pigmentosa
Amaurosis
Leber's hereditary optic neuropathy
Cone-rod dystrophy
Cone-rod dystrophy
Stargardt disease
Blindness
Bardet Biedl Syndrome
Corneal dystrophy
Human eye
Open angle glaucoma
Macular edema
CSNB
Endophthalmitis
Keratoconus
Eye disease
Electroretinogram
Vision loss
Penetrating keratoplasty
Visual impairment
Choroideremia
Retinal detachment
Optic neuropathy
Visual field
Diabetic retinopathy
Cataract
more...
Diseases and disorders
(27)
Anonychia onychodystrophy
Age related macular degeneration
Physiologic nystagmus
Usher syndrome
Degenerative diseases
Degenerative diseases
Joubert syndrome
Pupillary
Amelogenesis imperfecta
Achromatopsia
Microphthalmia
Strabismus
Rare diseases
Amblyopia
Retinitis pigmentosa
Amaurosis
Leber's hereditary optic neuropathy
Cone-rod dystrophy
Stargardt disease
Blindness
Bardet Biedl Syndrome
Open angle glaucoma
Keratoconus
Choroideremia
Retinal detachment
Optic neuropathy
Diabetic retinopathy
Cataract
more...
Chromosome 14 (human)
RPGRIP1
RDH12
SPATA7
Vision
Retinal
Night blindness
Ophthalmology
Age related macular degeneration
Physiologic nystagmus
Visual field
Amblyopia
Eye
(12)
Photoreceptor cell
Rhodopsin
Retina
Retinal pigment epithelium
Anterior segment
Anterior segment
Ophthalmology
Physiologic nystagmus
Human eye
Macular edema
Eye disease
Pupillary
Choroideremia
more...
Genetic disorders
(11)
Nephronophthisis
Genetic diseases
Retinitis pigmentosa
Leber's hereditary optic neuropathy
Bardet Biedl Syndrome
Bardet Biedl Syndrome
CSNB
Usher syndrome
Joubert syndrome
Amelogenesis imperfecta
Choroideremia
Microphthalmia
more...
Medical genetics
Gene therapy
Genetic counseling
Genetic diseases
Visual disturbances and blindness
(16)
Achromatopsia
Age related macular degeneration
Amblyopia
Asthenopia
Binasal hemianopsia
Binasal hemianopsia
Bitemporal hemianopsia
Blindness
Color blindness
Diplopia
Eyeborg
Hemeralopia
Low vision
Night blindness
Photophobia
Scintillating scotoma
Scotoma
more...
Medicine
Theodore Leber
Neovascular
Orphanet
Arch. Ophthalmol.
Diseases and disorders
Genetics
Gene
Gene transfer
X linked
Mutations
Genetic diseases
Gene
(12)
RPE65
AIPL1
CRB1
CEP290
PRPF31
PRPF31
LRAT
NR2E3
TULP1
FOXC1
RPGRIP1
RDH12
SPATA7
more...
Vision disorder
Monochromacy
Oguchi disease
Quadrantanopia
Low vision
Photophobia
Scintillating scotoma
Scotoma
See also
(20)
GUCY2D
Liquid crystal
ABCA4
IMPDH1
Autosomal recessive
Autosomal recessive
Visual cycle
Photoreceptor cells
Retinal gene therapy using lentiviral vectors
Stomach fundus
Retinal diseases
Autosomal dominant
Hum. Mol. Genet.
Lucentis
Congenital
Adeno-associated virus
Kelling
Nat. Genet.
Am. J. Hum. Genet.
Intravitreal
Guanylate cyclase
more...
more categories...
Health Providers & Organizations
›
Vitals.com
