Informaţii despre

Nume Retinoschisis 1, X-Linked, Juvenile
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation of retina
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Achromatopsia 3 Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bietti Crystalline Corneoretinal Dystrophy Bleeding Disorder, Platelet-Type, 11 Blessig's Cysts Blood Group--Ahonen Brain Small Vessel Disease with or Without Ocular Anomalies Bullous Retinoschisis Choroid Disease Choroideremia Choroiditis Chromosomal Triplication Coats Disease Color Vision Deficiency Combined Hamartoma of the Retina and Retinal Pigment Epithelium Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone Dystrophy Cone-Rod Dystrophy 2 Congenital Stationary Night Blindness Enhanced S-Cone Syndrome Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fundus Albipunctatus Goldmann-Favre Syndrome Grouped Pigmentation of the Retina Head Injury Hepatic Adenomas, Familial Hereditary Night Blindness Hydrops, Lactic Acidosis, and Sideroblastic Anemia Intermediate Uveitis Laryngoonychocutaneous Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 9 Lutheran Suppressor, X-Linked Macular Holes Melanoma Microcephaly Miyoshi Muscular Dystrophy 1 Myopia Neovascular Glaucoma Neuropathy Night Blindness Night Blindness, Congenital Stationary, Autosomal Dominant 2 Night Blindness, Congenital Stationary, Type 1e Night Blindness, Congenital Stationary, Type 2a Norrie Disease Papillorenal Syndrome Pars Planitis Pax2-Related Disorder Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Red-Green Color Blindness Refractive Error Retinal Degeneration Retinal Detachment Retinal Disease Retinal Telangiectasia Retinitis Retinitis Pigmentosa Retinoschisis, Autosomal Dominant Retinoschisis of Fovea Reye Syndrome Sensorineural Hearing Loss Shaken Baby Syndrome Sjogren-Larsson Syndrome Spondyloepiphyseal Dysplasia Congenita Stargardt Disease Stargardt Disease 1 Steroid-Induced Glaucoma Stickler Syndrome Strabismus Thrombosis Undifferentiated Pleomorphic Sarcoma Uveitis Vitreous Detachment X-Linked Congenital Stationary Night Blindness Yemenite Deaf-Blind Hypopigmentation Syndrome