Informaţii despre

Nume Retinal Degeneration
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale ochiului
Boli din aceeaşi familie Late-Onset Retinal Degeneration

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Aceruloplasminemia Achromatopsia Achromatopsia 2 Achromatopsia 3 Acute Zonal Occult Outer Retinopathy Adrenomyodystrophy Aging Albinism Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Autoimmune Retinopathy Autosomal Dominant Cerebellar Ataxia Autosomal Dominant Congenital Stationary Night Blindness Azoospermia Bardet-Biedl Syndrome Bardet-Biedl Syndrome 7 Bestrophinopathy Birdshot Chorioretinopathy Blepharospasm Blessig's Cysts Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Butterfly-Shaped Pigment Dystrophy Cancer-Associated Retinopathy Carotid Artery Occlusion Cataract Central Serous Chorioretinopathy Cerebellar Hypoplasia Cerebritis Ceroid Lipofuscinosis, Neuronal, 2 Ceroid Lipofuscinosis, Neuronal, 6 Ceroid Lipofuscinosis, Neuronal, 7 Chops Syndrome Choroidal Dystrophy, Central Areolar, 1 Choroideremia Choroiditis Ciliopathy Cleft Palate, Isolated Coats Disease Cockayne Syndrome Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 6 Congenital Stationary Night Blindness Cystic Kidney Disease Dementia Dermatitis Diabetes Mellitus Down Syndrome Endotheliitis Enhanced S-Cone Syndrome Epilepsy Epilepsy, Pyridoxine-Dependent Epithelial Recurrent Erosion Dystrophy Esterase C Ewing Sarcoma Eye Degenerative Disease Familial Hemiplegic Migraine Fundus Albipunctatus Fundus Dystrophy Glycogen Storage Disease Ii Goldmann-Favre Syndrome Hemiplegic Migraine Hepatitis Hereditary Ataxia Hereditary Choroidal Atrophy Hereditary Retinal Dystrophy Hereditary Spastic Paraplegia Homocystinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypotrichosis Hypoxia Infantile Cerebellar-Retinal Degeneration Infertility Ischemia Keratoconus Knobloch Syndrome Late-Onset Retinal Degeneration Late-Onset Retinal Degenration Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 9 Letterer-Siwe Disease Light Chain Deposition Disease Lipodystrophy, Congenital Generalized, Type 2 Machado-Joseph Disease Macroglobulinemia Macular Degeneration, Age-Related, 1 Macular Dystrophy, Dominant Cystoid Macular Dystrophy, Vitelliform, 3 Mccune-Albright Syndrome Melanoma-Associated Retinopathy Microcephaly Microphthalmia Motion Sickness Mucopolysaccharidoses Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Iiib Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Sulfatase Deficiency Myopathy Myopia Nephronophthisis Nephronophthisis 3 Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Nevus Comedonicus Nicolaides-Baraitser Syndrome Night Blindness Night Blindness, Congenital Stationary, Type 1a Ocular Albinism Ocular Hypertension Oliver-Mcfarlane Syndrome Olivopontocerebellar Atrophy Osteopetrosis Pancreatitis, Hereditary Paraplegia Partial Central Choroid Dystrophy Periodontitis Peripheral Retinal Degeneration Pineal Parenchymal Tumor of Intermediate Differentiation Pituitary Tumors Polycystic Kidney Disease Polydactyly Primary Congenital Glaucoma Primary Progressive Multiple Sclerosis Prolonged Electroretinal Response Suppression Pseudoxanthoma Elasticum Radin Blood Group Antigen Red-Green Color Blindness Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Cone Dystrophy 1 Retinal Detachment Retinal Disease Retinal Vascular Disease Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 2 Retinitis Pigmentosa 27 Retinitis Pigmentosa 3 Retinitis Pigmentosa 7 Rhyns Syndrome Senior-Løken Syndrome Severe Early-Childhood-Onset Retinal Dystrophy Smith-Lemli-Opitz Syndrome Solar Retinopathy Sotos Syndrome 1 Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spinocerebellar Ataxia 7 Spinocerebellar Atrophy Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Stickler Syndrome Transcobalamin Ii Deficiency Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina Usher Syndrome Usher Syndrome, Type I Usher Syndrome, Type if Usher Syndrome, Type Iic Usher Syndrome, Type Iid Uveitis Vascular Disease Vitelliform Macular Dystrophy Vitreoretinopathy, Neovascular Inflammatory Yemenite Deaf-Blind Hypopigmentation Syndrome