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Nume Macular Degeneration, Age-Related, 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale ochiului
Boli din aceeaşi familie Macular Degeneration, Age-Related, 10; Macular Degeneration, Age-Related, 11; Macular Degeneration, Age-Related, 12; Macular Degeneration, Age-Related, 13; Macular Degeneration, Age-Related, 14; Macular Degeneration, Age-Related, 15; Macular Degeneration, Age-Related, 2; Macular Degeneration, Age-Related, 4; Macular Degeneration, Age-Related, 5; Macular Degeneration, Age-Related, 6; Macular Degeneration, Age-Related, 7; Macular Degeneration, Age-Related, 8; Macular Degeneration, Age-Related, 9

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Boli A-Z Aarskog-Scott Syndrome Achromatopsia Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acute Hemorrhagic Leukoencephalitis Adie Pupil Adrenomyodystrophy Aging Aicardi-Goutieres Syndrome Aicardi-Goutieres Syndrome 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amblyopia Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Angioid Streaks Angiokeratoma Circumscriptum Aniridia 1 Anorexia Nervosa 1 Anterior Uveitis Aortic Valve Disease 2 Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Atherosclerosis Susceptibility Atrial Fibrillation Autoimmune Retinopathy Autosomal Dominant Congenital Stationary Night Blindness Bardet-Biedl Syndrome Basal Laminar Drusen Bestrophinopathy Best Vitelliform Macular Dystrophy Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Globoside 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 Breast Carcinoma in Situ C3 Glomerulopathy Cancer-Associated Retinopathy Capillary Hemangioma Carotenemia Carotid Artery Disease Cataract Cataract-Glaucoma Central Retinal Artery Occlusion Central Serous Chorioretinopathy Cerebellofaciodental Syndrome Cerebritis Charles Bonnet Syndrome Chlamydia Chorioamnionitis Chorioretinitis Choroiditis Chronic Myocardial Ischemia Complement Component 3 Deficiency, Autosomal Recessive Complement Factor B Deficiency Complement Factor D Deficiency Complement Factor H Deficiency Complement Factor I Deficiency Cone Dystrophy Cone-Rod Dystrophy 2 Congenital Stationary Night Blindness Corneal Dystrophy, Fleck Corneal Dystrophy, Posterior Polymorphous, 1 Corneal Neovascularization Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa Cytomegalovirus Retinitis Degeneration of Macula and Posterior Pole Degenerative Myopia Dementia De Novo Thrombotic Microangiopathy After Kidney Transplantation Dense Deposit Disease Diabetes Mellitus Diabetic Macular Edema Diencephalic Syndrome Doyne Honeycomb Retinal Dystrophy Dry Eye Syndrome Dysbaric Osteonecrosis Eales Disease Ectodermal Dysplasia Endophthalmitis Endotheliitis Enterocolitis Epithelioid Hemangioendothelioma Ewing Sarcoma Exfoliation Syndrome Extrinsic Cardiomyopathy Familial Drusen Fanconi Anemia, Complementation Group E Fanconi Anemia, Complementation Group G Frontotemporal Dementia, Chromosome 3-Linked Fundus Albipunctatus Fundus Dystrophy Gigantism Glomerulonephritis Glycogen Storage Disease Ii Haemophilus Influenzae Hantavirus Pulmonary Syndrome Hellp Syndrome Hemolytic-Uremic Syndrome Hemolytic Uremic Syndrome, Atypical 1 Hepatic Adenomas, Familial Hepatitis Hereditary Choroidal Atrophy Histoplasmosis Homozygous Familial Hypercholesterolemia Human Immunodeficiency Virus Type 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypolipoproteinemia Hypotrichosis Hypoxia Ichthyosis Impotence Kuhnt-Junius Degeneration Labyrinthitis Laryngitis Late-Onset Retinal Degeneration Leber Congenital Amaurosis Leber Congenital Amaurosis 4 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limb Ischemia Lupus Erythematosus Lyme Disease Lymphangioma Macular Degeneration, Age-Related, 10 Macular Degeneration, Age-Related, 11 Macular Degeneration, Age-Related, 12 Macular Degeneration, Age-Related, 13 Macular Degeneration, Age-Related, 14 Macular Degeneration, Age-Related, 15 Macular Degeneration, Age-Related, 2 Macular Degeneration, Age-Related, 4 Macular Degeneration, Age-Related, 5 Macular Degeneration, Age-Related, 6 Macular Degeneration, Age-Related, 7 Macular Degeneration, Age-Related, 8 Macular Degeneration, Age-Related, 9 Macular Degeneration, Early-Onset Macular Dystrophy, Dominant Cystoid Macular Dystrophy, Vitelliform, 2 Macular Dystrophy, Vitelliform, 3 Macular Holes Macular Retinal Edema Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Microvascular Complications of Diabetes 1 Microvascular Complications of Diabetes 5 Multifocal Choroiditis Mungan Syndrome Myocardial Infarction Myopia Myopic Macular Degeneration Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Olivopontocerebellar Atrophy Open-Angle Glaucoma Optic Disk Drusen Parametritis Parkinsonism with Spasticity, X-Linked Partial Central Choroid Dystrophy Patterned Macular Dystrophy Peripheral Retinal Degeneration Phacolytic Glaucoma Pinguecula Placenta Accreta Placental Insufficiency Plague Pneumonia Poems Syndrome Polyposis, Gastric Posttransplant Acute Limbic Encephalitis Proliferative Glomerulonephritis Prolonged Electroretinal Response Suppression Pseudomembranous Conjunctivitis Pseudoxanthoma Elasticum Purulent Labyrinthitis Pyelonephritis Radiation Proctitis Radin Blood Group Antigen Red-Green Color Blindness Refractive Error Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Degeneration Retinal Detachment Retinal Disease Retinal Drusen Retinal Vascular Disease Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 12 Retinitis Pigmentosa 19 Retinitis Pigmentosa 25 Rheumatoid Arthritis Rhyns Syndrome Scotoma Senile Cataract Severe Early-Childhood-Onset Retinal Dystrophy Sjogren-Larsson Syndrome Smith-Lemli-Opitz Syndrome Sotos Syndrome 1 Spasticity Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Sveinsson Chorioretinal Atrophy Systemic Lupus Erythematosus Tangier Disease Tay-Sachs Disease Thyroiditis Undifferentiated Pleomorphic Sarcoma Uveitis Vascular Cancer Vascular Disease Vitamin E, Familial Isolated Deficiency of Vitelliform Macular Dystrophy Vitreous Detachment Vitreous Disease Xanthoma Disseminatum Yemenite Deaf-Blind Hypopigmentation Syndrome