Informaţii despre

Nume Cone-Rod Dystrophy 2
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Cord compression, unspecified; Hereditary retinal dystrophy
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale

Vezi şi

Boli A-Z Achromatopsia Achromatopsia 3 Achromatopsia 4 Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Blood Group--Ahonen Cataract Chorioretinitis Choroidal Dystrophy, Central Areolar, 1 Choroid Disease Choroideremia Choroiditis Chylomicron Retention Disease Cleft Lip Color Blindness Cone Dystrophy Cone-Rod Dystrophy 1 Cone-Rod Dystrophy 12 Cone-Rod Dystrophy 17 Cone-Rod Dystrophy 3 Cone-Rod Dystrophy 6 Cone-Rod Dystrophy 7 Cone-Rod Dystrophy 8 Cone-Rod Dystrophy 9 Cone-Rod Dystrophy and Hearing Loss Cone-Rod Dystrophy, X-Linked, 1 Cone-Rod Dystrophy, X-Linked, 3 Congenital Stationary Night Blindness Cortisone Reductase Deficiency 1 Danon Disease Degeneration of Macula and Posterior Pole Eye Degenerative Disease Fundus Albipunctatus Fundus Dystrophy Growth Hormone Deficiency Hereditary Ataxia Hereditary Choroidal Atrophy Hereditary Night Blindness Hereditary Retinal Dystrophy Jalili Syndrome Keratoconus Keratomalacia Laurence-Moon Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 9 Limb-Girdle Muscular Dystrophy Macular Degeneration, Age-Related, 1 Megaloblastic Anemia Muscular Dystrophy Myopia Nephronophthisis Nephronophthisis 4 Neurofibromatosis, Type Iv, of Riccardi Night Blindness Night Blindness, Congenital Stationary, Type 1a Occult Macular Dystrophy Oligocone Trichromacy Partial Central Choroid Dystrophy Peripheral Retinal Degeneration Prolonged Electroretinal Response Suppression Radin Blood Group Antigen Red-Green Color Blindness Refsum Disease, Classic Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Degeneration Retinal Disease Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 2 Retinitis Pigmentosa 26 Retinitis Pigmentosa 3 Retinoschisis 1, X-Linked, Juvenile Rhyns Syndrome Scotoma Severe Early-Childhood-Onset Retinal Dystrophy Solar Retinopathy Spinocerebellar Ataxia 7 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Tetraamelia Syndrome, Autosomal Recessive Thiamine-Responsive Megaloblastic Anemia Syndrome Tritanopia Yemenite Deaf-Blind Hypopigmentation Syndrome