Informaţii despre

Nume Retinal Disease
Pagina Web www.malacards.org
Clasificari ICD10 Other specified retinal disorders; Retinal disorder, unspecified
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z Achromatopsia Achromatopsia 2 Achromatopsia 3 Achromatopsia 4 Acute Zonal Occult Outer Retinopathy Adrenomyodystrophy Aging Aland Island Eye Disease 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 Alzheimer Disease 3 Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Autosomal Dominant Congenital Stationary Night Blindness Bardet-Biedl Syndrome 5 Bestrophinopathy Best Vitelliform Macular Dystrophy Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blue Cone Monochromacy Butterfly-Shaped Pigment Dystrophy C3 Glomerulopathy Cancer-Associated Retinopathy Cataract Central Serous Chorioretinopathy Cerebritis Charles Bonnet Syndrome Chorioretinitis Choroidal Dystrophy, Central Areolar, 1 Choroideremia Choroiditis Coats Disease Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 3 Cone-Rod Dystrophy 6 Congenital Stationary Night Blindness Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 23 Degeneration of Macula and Posterior Pole Dementia Dense Deposit Disease Dfnb1 Diabetes Mellitus Endotheliitis Enhanced S-Cone Syndrome Ewing Sarcoma Eye Degenerative Disease Focal Chorioretinitis Fundus Albipunctatus Fundus Dystrophy Glycogen Storage Disease Ii Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hereditary Choroidal Atrophy Hereditary Night Blindness Hereditary Retinal Dystrophy Herpes Simplex Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoxia Insulin-Like Growth Factor I Jalili Syndrome Keratoconus Kuhnt-Junius Degeneration Laurence-Moon Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 10 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 3 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 9 Lupus Erythematosus Macular Degeneration, Age-Related, 1 Macular Dystrophy, Vitelliform, 3 Macular Holes Marfan Syndrome Melanoma-Associated Retinopathy Multifocal Choroiditis Necrobiosis Lipoidica Neovascular Glaucoma Neuritis Neuronitis Night Blindness Night Blindness, Congenital Stationary, Type 1b Night Blindness, Congenital Stationary, Type 1e Night Blindness, Congenital Stationary, Type 2a Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis Occult Macular Dystrophy Ocular Hypertension Oligocone Trichromacy Optic Nerve Disease Optic Neuritis Orofaciodigital Syndrome I Partial Central Choroid Dystrophy Peripheral Retinal Degeneration Prolonged Electroretinal Response Suppression Radin Blood Group Antigen Red-Green Color Blindness Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Degeneration Retinal Detachment Retinal Drusen Retinal Telangiectasia Retinal Vascular Disease Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 13 Retinitis Pigmentosa 26 Retinitis Pigmentosa 3 Retinitis Pigmentosa 44 Retinitis Pigmentosa 50 Retinitis Pigmentosa 7 Retinoblastoma Retinoschisis 1, X-Linked, Juvenile Rhyns Syndrome Rubella Serpiginous Choroiditis Severe Early-Childhood-Onset Retinal Dystrophy Sleep Apnea Spasmus Nutans Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Systemic Lupus Erythematosus Usher Syndrome Usher Syndrome Type 2 Usher Syndrome, Type I Usher Syndrome, Type Id Usher Syndrome, Type if Usher Syndrome, Type Ig Usher Syndrome, Type Iic Usher Syndrome, Type Iid Usher Syndrome, Type Iiia Uveitis Vaginitis Vitelliform Macular Dystrophy Vitreoretinopathy, Neovascular Inflammatory Vitreous Detachment X-Linked Congenital Stationary Night Blindness Yemenite Deaf-Blind Hypopigmentation Syndrome