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Cone-rod Dystrophy
Cone-rod dystrophy
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Ophthalmology
(17)
Retinopathy
Retinitis pigmentosa
Leber congenital amaurosis
Stargardt disease
Corneal dystrophy
Corneal dystrophy
Bardet Biedl Syndrome
Eye disease
Retinitis
Retinoschisis
Electroretinography
Open angle glaucoma
Retinal detachment
Visual field
Choroideremia
Progressive retinal atrophy
Retinal dysplasia
Loss of vision
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Diseases and disorders
(28)
Salaam seizures
Cutis hyperelastica
Conns Syndrome
Mycobacterial
Corpus callosum agenesis
Corpus callosum agenesis
Cushings syndrome
Muscular dystrophy
Achromatopsia
Retinococh- leocerebral vasculopathy
Blue cone monochromatism
Amelogenesis imperfecta
Polydactyly
Best disease
Physiologic nystagmus
Alstrom syndrome
Day blindness
Usher syndrome
Degenerative diseases
Cutis laxa
Color blindness
Retinitis pigmentosa
Leber congenital amaurosis
Stargardt disease
Bardet Biedl Syndrome
Retinoschisis
Open angle glaucoma
Retinal detachment
Choroideremia
more...
Congenital disorders
Camptodactyly
Cutis hyperelastica
Corpus callosum agenesis
Polydactyly
Genetic disorders
(13)
Nephronophthisis
Inherited disorder
Laurence Moon syndrome
Cutis hyperelastica
Muscular dystrophy
Muscular dystrophy
Retinitis pigmentosa
Bardet Biedl Syndrome
Amelogenesis imperfecta
Polydactyly
Alstrom syndrome
Choroideremia
Usher syndrome
Color blindness
more...
Photoreceptor cells
Photoreceptor cell
Retinal
Retinal cone
Rod cells
Dehydroretinal
Outer segment disc shedding
Photosensitive ganglion cell
Eye
(14)
Rhodopsin
Retina
Retinitis Pigmentosa International
Scotopic
Fovea
Fovea
Optic disc
Dark adaptation
Photoreceptor cell
Retinal cone
Eye disease
Rod cells
Physiologic nystagmus
Day blindness
Choroideremia
more...
Visual disturbances and blindness
(16)
Night blindness
Photophobia
Achromatopsia
Amblyopia
Asthenopia
Asthenopia
Binasal hemianopsia
Bitemporal hemianopsia
Blindness
Color blindness
Day blindness
Diplopia
Eyeborg
Low vision
Macular degeneration
Scintillating scotoma
Scotoma
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Genes on chromosome 1
NPHP4
GNAT2
RPE65
CRB1
USH2A
MYOC
Genetics
Gene
X linked
Gene mutation
Inherited disorder
Gene
(15)
GUCA1A
RPGRIP1
NR2E3
PRPF31
CRX (gene)
CRX (gene)
RLBP1
Peripherin
RDH12
AIPL1
NPHP4
GNAT2
RPE65
CRB1
USH2A
MYOC
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See also
(20)
Conjugated bilirubin
Wire-haired
Norwegian School of Veterinary Science
ABCA4
CNGB3
CNGB3
Autosomal dominant
Autosomal recessive
Stomach fundus
GUCY2D
Cone monochromacy
Molday
Genome Research
Dryja, Greater Poland Voivodeship
CNGA3
Cone valve
Cinder Cone (volcano)
Chromosome 5
Dichromacy
Color vision
Foundation Fighting Blindness
more...
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