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Nume Retinitis
Pagina Web www.malacards.org
Clasificari ICD10 Chorioretinal inflammation, unspecified
Clasificare anatomică Malacards Eye diseases

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Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 48,xxyy Syndrome Abdominal Tuberculosis Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Abnormal Retinal Correspondence Accessory Mitral Valve Tissue Accommodative Esotropia Aceruloplasminemia Achondroplasia Achromatopsia Acquired Immunodeficiency Syndrome Acquired Thrombocytopenia Acromegaly Acute Closed-Angle Glaucoma Acute Lymphocytic Leukemia Acute Macular Neuroretinopathy Acute Mountain Sickness Acute Myocardial Infarction Acute Posterior Multifocal Placoid Pigment Epitheliopathy Acute Retinal Necrosis Syndrome Acute Zonal Occult Outer Retinopathy Adenocarcinoma Adenoma Adenosine Deaminase 2 Deficiency Adrenomyodystrophy Adult T-Cell Leukemia Aging Aicardi Syndrome Alagille Syndrome 1 Aland Island Eye Disease Albinism Albinism, Ocular, Type I Allergic Conjunctivitis Allergic Encephalomyelitis Alopecia Alopecia Areata 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 Amaurosis Fugax Amblyopia Amyloidosis Anauxetic Dysplasia 1 Anca-Associated Vasculitis Androgen Insensitivity, Partial Aneurysm Angioid Streaks Angioma Serpiginosum Angiomatosis Aniridia 1 Aniseikonia Anisometropia Anorexia Nervosa 1 Anoxia Anterior Uveitis Antiphospholipid Syndrome Antithrombin Iii Deficiency Aplasia Cutis Congenita Aplastic Anemia Apparent Mineralocorticoid Excess Aqueous Misdirection Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Aspergillosis Asphyxiating Thoracic Dystrophy Astigmatism Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Atrial Fibrillation Autoimmune Retinopathy Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Cerebellar Ataxia Autosomal Dominant Disease Autosomal Dominant Optic Atrophy, Classic Form Autosomal Dominant Polycystic Kidney Disease Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Non-Syndromic Intellectual Disability Axenfeld-Rieger Syndrome Azoospermia Babesiosis Background Diabetic Retinopathy Bardet-Biedl Syndrome Bardet-Biedl Syndrome 10 Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 4 Bardet-Biedl Syndrome 8 Basal Cell Carcinoma B-Cell Lymphomas Bestrophinopathy Bestrophinopathy, Autosomal Recessive Best Vitelliform Macular Dystrophy Bietti Crystalline Corneoretinal Dystrophy Bilateral Retinoblastoma Birdshot Chorioretinopathy Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Blau Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blepharospasm Blessig's Cysts Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System Body Dysmorphic Disorder 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borna Disease Bornholm Eye Disease Boucher-Neuhauser Syndrome Brachydactyly Brachymorphism-Onychodysplasia-Dysphalangism Syndrome Brain Injury Brain Small Vessel Disease with or Without Ocular Anomalies Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Breast Cancer Brittle Bone Disorder Brody Myopathy Bronchiectasis Butterfly-Shaped Pigment Dystrophy C3 Glomerulopathy Calcinosis Cancer-Associated Retinopathy Candidiasis Capillary Hemangioma Carney Complex Variant Carnosinemia Carotid Artery Disease Carotid Artery Dissection Carotid Artery Occlusion Carotid Stenosis Cataract Cataract 5, Multiple Types Catastrophic Antiphospholipid Syndrome Cat-Scratch Disease Cavernous Hemangioma Cavernous Malformation Cavernous Sinus Thrombosis Cellulitis Central Nervous System Disease Central Nervous System Lymphoma Central Nervous System Tuberculosis Central Nervous System Vasculitis Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebellar Degeneration Cerebellar Hypoplasia Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Artery Occlusion Cerebral Atrophy Cerebral Cavernous Malformations Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 2 Ceroid Lipofuscinosis, Neuronal, 6 Ceroid Lipofuscinosis, Neuronal, 7 Cervicitis Chagas Disease Charles Bonnet Syndrome Chediak-Higashi Syndrome Chiasmal Syndrome Chickenpox Chlamydia Cholecystitis Cholelithiasis Cholera Cholestasis Chondrodysplasia Punctata Syndrome Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choriocarcinoma Chorioretinal Scar Chorioretinitis Choroideremia Choroiditis Christianson Syndrome Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 6q Deletion Chronic Closed-Angle Glaucoma Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Progressive External Ophthalmoplegia Churg-Strauss Syndrome Ciliary Dyskinesia, Primary, 1 Ciliopathy Cinca Syndrome Cluster Headache Coats Disease Coccidioidomycosis Cockayne Syndrome Cogan Syndrome Cohen Syndrome Colitis Coloboma of Optic Nerve Color Blindness Colorectal Cancer Color Vision Deficiency Combined Hamartoma of the Retina and Retinal Pigment Epithelium Common Cold Common Variable Immunodeficiency Complement Factor B Deficiency Complement Factor H Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone Dystrophy Cone-Rod Dystrophy 16 Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 21 Cone-Rod Dystrophy 5 Cone-Rod Dystrophy 6 Cone-Rod Dystrophy 7 Congenital Cytomegalovirus Congenital Hepatic Fibrosis Congenital Herpes Simplex Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Nystagmus Congenital Retinal Arteriovenous Communication Congenital Stationary Night Blindness Congenital Toxoplasmosis Conjunctival Squamous Cell Carcinoma Conjunctivitis Conn's Syndrome Connective Tissue Disease Conotruncal Heart Malformations Corneal Edema Corneal Neovascularization Corneal Staphyloma Cortical Blindness Costello Syndrome Cowden Disease Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Crest Syndrome Crohn's Colitis Crohn's Disease Cryofibrinogenemia Cryoglobulinemia Cryptorchidism, Unilateral or Bilateral Cutis Laxa Cutis Laxa, Autosomal Recessive, Type Iiia Cutis Marmorata Telangiectatica Congenita Cutis Verticis Gyrata Cysticercosis Cystic Fibrosis Cystic Kidney Disease Cystinosis Cystinuria Cytomegalic Inclusion Disease Cytomegalovirus Infection Cytomegalovirus Retinitis Dacryocystitis Danon Disease D-Bifunctional Protein Deficiency Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Degenerative Myopia Dementia Dengue Hemorrhagic Fever Dense Deposit Disease Dental Abscess Dermatitis Dermatomyositis Desmosterolosis Dextrocardia Diabetes and Deafness, Maternally Inherited Diabetes Insipidus Diabetes Mellitus Diabetic Cataract Diabetic Foot Ulcers Diabetic Macular Edema Diabetic Neuropathy Diabetic Polyneuropathy Digeorge Syndrome Dilated Cardiomyopathy Discoid Lupus Erythematosus Donnai-Barrow Syndrome Down Syndrome Doyne Honeycomb Retinal Dystrophy Duane-Radial Ray Syndrome Duane Retraction Syndrome Duane Retraction Syndrome 1 Dwarfism Dysautonomia Dyskeratosis Congenita Dyskeratosis Congenita Autosomal Dominant Eales Disease Early Myoclonic Encephalopathy Eclampsia Ectodermal Dysplasia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 Eisenmenger Syndrome Elliptocytosis 2 Embryonal Rhabdomyosarcoma Empty Sella Syndrome Encephalitis Encephalocele Encephalomalacia Encephalomyopathy Encephalopathy Endocarditis Endophthalmitis Endotheliitis End Stage Renal Failure Enhanced S-Cone Syndrome Entropion Eosinophilic Granulomatosis with Polyangiitis Eosinophilic Pneumonia Ependymoma Epilepsy Epilepsy, Pyridoxine-Dependent Epileptic Encephalopathy, Early Infantile, 3 Epileptic Encephalopathy, Early Infantile, 4 Epithelial Recurrent Erosion Dystrophy Epulis Equatorial Staphyloma Erysipelas Esotropia Essential Iris Atrophy Essential Thrombocythemia Esterase C Ethmoid Sinus Adenocarcinoma Exfoliation Syndrome Exotropia Extracranial Carotid Artery Aneurysm Exudative Vitreoretinopathy Exudative Vitreoretinopathy 1 Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor Vii Deficiency Factor Xi Deficiency Factor Xii Deficiency Familial Adenomatous Polyposis Familial Adenomatous Polyposis 1 Familial Colorectal Cancer Familial Drusen Familial Hemiplegic Migraine Familial Mediterranean Fever Familial Retinoblastoma Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fatty Liver Disease Fetal Alcohol Syndrome Fibromuscular Dysplasia Focal Dermal Hypoplasia Focal Segmental Glomerulosclerosis Foot Drop Foster-Kennedy Syndrome Fourth Cranial Nerve Palsy Frenkel Russe Syndrome Friedreich Ataxia 1 Fuchs' Heterochromic Uveitis Fundus Albipunctatus Fundus Dystrophy Galactose Epimerase Deficiency Galactosemia Galactosialidosis Gapo Syndrome Gastric Adenocarcinoma Gastric Cancer Gastrointestinal Stromal Tumor Gastroschisis Gerstmann Syndrome Gestational Diabetes Giardioză Gigantism Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glaucomatocyclitic Crisis Glioma Glomerulonephritis Glutathione Synthetase Deficiency Glycogen Storage Disease Ii Goldmann-Favre Syndrome Good Syndrome Gout Graft-Versus-Host Disease Granulocytopenia Granuloma Annulare Granulomatous Angiitis Griscelli Syndrome Grouped Pigmentation of the Retina Growth Hormone Deficiency Gurrieri Syndrome Gyrate Atrophy of Choroid and Retina Haim-Munk Syndrome Hairy Cell Leukemia Hallermann-Streiff Syndrome Hansen's Disease Hawkinsinuria Headache Head Injury Helix Syndrome Hellp Syndrome Hemangioblastoma Hemangioma Hematopoietic Stem Cell Transplantation Hemifacial Atrophy, Progressive Hemiplegia Hemiplegic Migraine Hemochromatosis, Neonatal Hemoglobin C Disease Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia B Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemosiderosis Heparin Cofactor Ii Deficiency Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Amyloidosis Hereditary Ataxia Hereditary Hemorrhagic Telangiectasia Hereditary Retinal Dystrophy Hereditary Spastic Paraplegia Hereditary Spherocytosis Heritable Pulmonary Arterial Hypertension Hermansky-Pudlak Syndrome Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpes Zoster Ophthalmicus Heterotaxy, Visceral, 2, Autosomal Histiocytosis Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Holoprosencephaly Homocarnosinosis Homocystinuria Human Immunodeficiency Virus Type 1 Hydranencephaly Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hyperostosis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertensive Retinopathy Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertropia Hyperuricemia Hypoaldosteronism Hypoascorbemia Hypoglycemia Hypogonadism Hypophosphatasia Hypopituitarism Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration Hypopyon Hypotonia Hypotrichosis Hypoxia Ichthyosis Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Idiopathic Juxtafoveal Retinal Telangiectasia Idiopathic Macular Telangiectasia Type 1 Idiopathic Macular Telangiectasia Type 3 Immunoglobulin E Concentration, Serum Incontinentia Pigmenti Infantile Cerebellar-Retinal Degeneration Infective Endocarditis Infertility Inflammatory Bowel Disease Inflammatory Bowel Disease 1 Influenza Insulin-Like Growth Factor I Intermediate Uveitis Interstitial Nephritis Intracranial Hypertension Intrahepatic Cholestasis Intraocular Lymphoma Intraocular Melanoma Intraocular Retinoblastoma Iridocorneal Endothelial Syndrome Iridocyclitis Iritis Iron Deficiency Anemia Irvan Syndrome Ischemia Ischemic Optic Neuropathy Ischemic Retinopathy Isolated Duane Retraction Syndrome Isolated Ectopia Lentis Isolated Growth Hormone Deficiency Isolated Optic Neuritis Juvenile Glaucoma Juvenile Nasopharyngeal Angiofibroma Juvenile Xanthogranuloma Kabuki Syndrome 1 Kawasaki Disease Kearns-Sayre Syndrome Keloids Keratitis, Hereditary Keratoconjunctivitis Keratoconus Keratomalacia Klippel-Trenaunay-Weber Syndrome Kniest Dysplasia Knobloch Syndrome Lactic Acidosis Langerhans Cell Histiocytosis Laryngitis Late-Onset Retinal Degeneration Late-Onset Retinal Degenration Lateral Sclerosis Laugier-Hunziker Syndrome Laurence-Moon Syndrome Learning Disability Leber Congenital Amaurosis Leber Congenital Amaurosis 14 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 5 Leber Hereditary Optic Neuropathy Legius Syndrome Lens Subluxation Letterer-Siwe Disease Leukemia Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukomalacia Leukostasis Lichen Planus Light Chain Deposition Disease Light Fixation Seizure Syndrome Linear Scleroderma Lipid Metabolism Disorder Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 Lissencephaly Livedoid Vasculopathy Liver Disease Loeys-Dietz Syndrome Loiasis Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Low Tension Glaucoma Lung Cancer Lung Cancer Susceptibility 3 Lupus Erythematosus Lutheran Suppressor, X-Linked Lyme Disease Lymphangioma Lymphoblastic Leukemia Lymphoma Lymphoma, Hodgkin, Classic Lymphoma, Mucosa-Associated Lymphoid Type Lymphomatoid Granulomatosis Lymphomatoid Papulosis Lymphoplasmacytic Lymphoma Lymphosarcoma Lysosomal Storage Disease Machado-Joseph Disease Macroglobulinemia Macrophage Activation Syndrome Macular Dystrophy, Dominant Cystoid Macular Dystrophy, Patterned, 1 Macular Dystrophy, Patterned, 3 Macular Dystrophy, Retinal, 1, North Carolina Type Macular Dystrophy, Vitelliform, 2 Macular Holes Major Affective Disorder 2 Malaria Malignant Histiocytosis Malignant Hypertension Malignant Hyperthermia 1 Mannosidosis Mannosidosis, Alpha B, Lysosomal Maple Syrup Urine Disease Marfan Syndrome Mast Cell Activation Syndrome Mccune-Albright Syndrome Mckusick-Kaufman Syndrome Mcleod Syndrome Medulloblastoma Medulloepithelioma Megaloblastic Anemia Megalocornea Melanoma Melanoma-Associated Retinopathy Melanotic Neuroectodermal Tumor Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningioma, Familial Meningitis Meningocele Meningoencephalitis Menkes Disease Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome Merkel Cell Carcinoma Metabolic Acidosis Methanol Poisoning Mevalonic Aciduria Microcephaly Microphthalmia Microscopic Polyangiitis Microtia-Anotia Migraine with Aura Migraine with or Without Aura 1 Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Mitochondrial Complex I Deficiency Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mixed Connective Tissue Disease Mixed Germ Cell Cancer Miyoshi Muscular Dystrophy 1 Mononeuritis Multiplex Morbid Obesity Morning Glory Syndrome Motion Sickness Moyamoya Disease 1 Mucolipidosis Iv Mucopolysaccharidoses Mucopolysaccharidosis Iii Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis, Type Iiib Mucopolysaccharidosis, Type Iiic Mulibrey Nanism Multifocal Choroiditis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Sulfatase Deficiency Multiple System Atrophy 1 Mumps Mungan Syndrome Muscle Eye Brain Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Congenital, Lmna-Related Myelitis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myhre Syndrome Myocardial Infarction Myopathy Myopia Myotonia Myotonia Atrophica Myotonic Dystrophy Nance-Horan Syndrome Nasopharyngitis Necrobiosis Lipoidica Necrotizing Fasciitis Neonatal Herpes Neovascular Glaucoma Nephrocalcinosis Nephronophthisis Nephronophthisis 3 Nephrosclerosis Nephrotic Syndrome Nervous System Disease Neuritis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurodermatitis Neurofibromatosis, Type Iv, of Riccardi Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neuropathy, Ataxia, and Retinitis Pigmentosa Neuroretinitis Neurosarcoidosis Neurosyphilis Neutrophil Actin Dysfunction Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Nevus of Ota Newfoundland Rod-Cone Dystrophy Nicolaides-Baraitser Syndrome Night Blindness Night Blindness, Congenital Stationary, Type 1a Nocardiosis Nonarteritic Anterior Ischemic Optic Neuropathy Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis Non-Involuting Congenital Hemangioma Non-Langerhans-Cell Histiocytosis Nonsyndromic Retinitis Pigmentosa Norrie Disease Nutritional Optic Neuropathy Occipital Horn Syndrome Occult Macular Dystrophy Ocular Albinism Ocular Hypertension Ocular Melanoma Ocular Toxoplasmosis Oculoauricular Syndrome Oculocutaneous Albinism Oculopharyngeal Muscular Dystrophy Oligodendroglioma Oliver-Mcfarlane Syndrome Olivopontocerebellar Atrophy Onchocerciasis Open-Angle Glaucoma Ophthalmomyiasis Optic Atrophy 3, Autosomal Dominant Optic Disk Drusen Optic Nerve Disease Optic Nerve Glioma Optic Nerve Hypoplasia, Bilateral Optic Neuritis Optic Papillitis Optic Pathway Glioma Optic Perineuritis Orbital Cancer Orbital Cellulitis Orbital Cyst Orbital Granuloma Orbital Lymphangioma Orbital Lymphoma Orbital Plasma Cell Granuloma Orbital Tenonitis Orbit Lymphoma Orchitis Osteochondrodysplasia Osteopetrosis Osteoporosis-Pseudoglioma Syndrome Ovalocytosis, Southeast Asian Ovarian Cancer Ovarian Hyperstimulation Syndrome Overhydrated Hereditary Stomatocytosis Pachygyria Paget's Disease of Bone Paget Disease of Bone 3 Pallister-Killian Mosaic Syndrome Pallister-Killian Syndrome Pancreatitis Pancytopenia Panic Disorder Panophthalmitis Panuveitis Papillary Carcinoma Papilledema Papilloma Papillon-Lefevre Syndrome Papillorenal Syndrome Paraplegia Paroxysmal Nocturnal Hemoglobinuria Pars Planitis Partial Arterial Retinal Occlusion Patent Foramen Ovale Pax2-Related Disorder Pediatric Multiple Sclerosis Penis Agenesis Perinephritis Periodontitis Peripheral Retinal Degeneration Periventricular Leukomalacia Pernicious Anemia Peroxisomal Biogenesis Disorders Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Pertussis Peters-Plus Syndrome Peutz-Jeghers Syndrome Pfeiffer Syndrome Phacolytic Glaucoma Phacomatosis Pigmentovascularis Phaeochromocytoma Phelan-Mcdermid Syndrome Phimosis Photosensitive Epilepsy Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked Pigmented Paravenous Chorioretinal Atrophy Pituitary Adenoma Pituitary Tumors Placental Insufficiency Plasminogen Deficiency, Type I Plasmodium Vivax Malaria Platelet Membrane Fluidity Pneumonia Poems Syndrome Polyarteritis Nodosa Polycystic Kidney Disease Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polydactyly Polymicrogyria Polymyositis Polyneuropathy Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Porencephaly Poretti-Boltshauser Syndrome Porphyria Posterior Cerebral Artery Infarction Posterior Column Ataxia Posterior Column Ataxia with Retinitis Pigmentosa Posterior Polar Cataract Posterior Scleritis Posterior Uveal Melanoma Posterior Uveitis Potocki-Lupski Syndrome Precursor T-Cell Acute Lymphoblastic Leukemia Pre-Eclampsia Premature Centromere Division Premature Chromatid Separation Trait Prepapillary Vascular Loops Preretinal Fibrosis Presbyopia Primary Angle-Closure Glaucoma Primary Central Nervous System Lymphoma Primary Ciliary Dyskinesia Primary Congenital Glaucoma Primary Hyperoxaluria Primary Lateral Sclerosis, Adult, 1 Primary Progressive Multiple Sclerosis Prion Disease Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Multifocal Leukoencephalopathy Proliferative Glomerulonephritis Prolonged Electroretinal Response Suppression Prolymphocytic Leukemia Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Proteus Syndrome Pseudohypoparathyroidism Pseudomyxoma Peritonei Pseudopapilledema Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Tuberculosis Punctate Inner Choroidopathy Purine Nucleoside Phosphorylase Deficiency Purpura Pyoderma Pyoderma Gangrenosum Pyogenic Granuloma Quadriplegia Radin Blood Group Antigen Ramon Syndrome Reactive Arthritis Refractive Error Refractory Anemia Refsum Disease, Classic Relapsing Polychondritis Relapsing-Remitting Multiple Sclerosis Renal Dysplasia Renal Tubular Acidosis Renovascular Hypertension Restless Legs Syndrome Restrictive Dermopathy, Lethal Reticular Dysgenesis Reticulum Cell Sarcoma Retinal Aplasia Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis Retinal Arteries, Tortuosity of Retinal Artery Occlusion Retinal Cancer Retinal Cone Dystrophy 1 Retinal Degeneration Retinal Detachment Retinal Disease Retinal Drusen Retinal Dystrophy and Obesity Retinal Dystrophy with or Without Macular Staphyloma Retinal Hemangioblastoma Retinal Ischemia Retinal Lattice Degeneration Retinal Microaneurysm Retinal Perforation Retinal Telangiectasia Retinal Vascular Disease Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinal Venous Beading Retina Lymphoma Retinitis Pigmentosa Retinitis Pigmentosa 1 Retinitis Pigmentosa 10 Retinitis Pigmentosa 11 Retinitis Pigmentosa 12 Retinitis Pigmentosa 13 Retinitis Pigmentosa 14 Retinitis Pigmentosa 17 Retinitis Pigmentosa 18 Retinitis Pigmentosa 19 Retinitis Pigmentosa 2 Retinitis Pigmentosa 22 Retinitis Pigmentosa 23 Retinitis Pigmentosa 24 Retinitis Pigmentosa 25 Retinitis Pigmentosa 26 Retinitis Pigmentosa 27 Retinitis Pigmentosa 28 Retinitis Pigmentosa 29 Retinitis Pigmentosa 3 Retinitis Pigmentosa 31 Retinitis Pigmentosa 33 Retinitis Pigmentosa 4 Retinitis Pigmentosa 45 Retinitis Pigmentosa 6 Retinitis Pigmentosa 7 Retinitis Pigmentosa 9 Retinitis Pigmentosa, Late-Adult Onset Retinoblastoma Retinochoroidal Coloboma Retinoschisis 1, X-Linked, Juvenile Retinoschisis, Autosomal Dominant Revesz Syndrome Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Rhyns Syndrome Richards-Rundle Syndrome Rift Valley Fever Ring Chromosome 13 Roberts Syndrome Robinow Syndrome, Autosomal Recessive Rocky Mountain Spotted Fever Rosai-Dorfman Disease Rubella Rubeosis Iridis Rud Syndrome Sacrococcygeal Teratoma Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoidosis 2 Sarcoma Scapuloperoneal Myopathy, Myh7-Related Schimmelpenning-Feuerstein-Mims Syndrome Schizophrenia Schwartz-Jampel Syndrome, Type 1 Scleral Staphyloma Scleritis Scleromalacia Perforans Scleromyxedema Scoliosis Scotoma Scrapie Seckel Syndrome Secondary Syphilis Seizures, Benign Familial Neonatal, 1 Senior-Boichis Syndrome Senior-Løken Syndrome Sensorineural Hearing Loss Serpiginous Choroiditis Severe Combined Immunodeficiency Severe Early-Childhood-Onset Retinal Dystrophy Severe Pre-Eclampsia Shaken Baby Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sickle Cell Disease Siderosis Simultanagnosia Sinusitis Situs Inversus Sjogren-Larsson Syndrome Skeletal Dysplasias Skin Melanoma Sleep Apnea Small Cell Carcinoma Smallpox Smith-Lemli-Opitz Syndrome Smith-Mccort Dysplasia 1 Sneddon Syndrome Solar Retinopathy Sotos Syndrome 1 Spasmus Nutans Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Quadriplegia Spinal Muscular Atrophy Spindle Cell Hemangioma Spinocerebellar Ataxia 7 Spinocerebellar Atrophy Splenomegaly Spondylitis Spondyloarthropathy 1 Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepimetaphyseal Dysplasia, Strudwick Type Spondyloepiphyseal Dysplasia Congenita Spondylometaphyseal Dysplasia, Axial Spondylometaphyseal Dysplasia, Sedaghatian Type Spotted Fever Squamous Cell Carcinoma Stargardt Disease Stargardt Macular Degeneration Steatorrhea Steroid-Induced Glaucoma Stickler Syndrome Stickler Syndrome, Type I, Nonsyndromic Ocular Stomatitis Storm Syndrome Strabismus Streptococcal Meningitis Sturge-Weber Syndrome Stuve-Wiedemann Syndrome Subacute Bacterial Endocarditis Subclavian Steal Syndrome Susac Syndrome Sveinsson Chorioretinal Atrophy Sympathetic Ophthalmia Syncope Synostosis Syphilis Systemic Lupus Erythematosus Tay-Sachs Disease T-Cell Leukemia T-Cell Prolymphocytic Leukemia Telangiectasis Temple-Baraitser Syndrome Temporal Arteritis Teratoma Testicular Regression Syndrome Tetraamelia Syndrome, Autosomal Recessive Tetralogy of Fallot Tetraploidy Thalassemia Thelaziasis Three M Syndrome 1 Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Thyroiditis Tinea Unguium Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxic Optic Neuropathy Toxocariasis Toxoplasmoză Transcobalamin Ii Deficiency Transient Retinal Arterial Occlusion Transverse Myelitis Traumatic Brain Injury Tremor Trichomegaly Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina Tritanopia Trnt1 Deficiency Tuberculoid Leprosy Tuberculous Uveitis Tuberous Sclerosis Tubulin, Beta Turner Syndrome Type Ii Mixed Cryoglobulinemia Typhoid Fever Ulcerative Colitis Ulnar Neuropathy Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and Brachydactyly Unilateral Retinoblastoma Usher Syndrome Usher Syndrome Type 2 Usher Syndrome, Type I Usher Syndrome, Type Ig Usher Syndrome, Type Iia Uveal Diseases Uveitis Vaginitis Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vasculopathy, Retinal, with Cerebral Leukodystrophy Vasoproliferative Tumor of the Retina Vernal Keratoconjunctivitis Vici Syndrome Viral Encephalitis Viral Meningitis Vitamin B12 Deficiency Vitelliform Macular Dystrophy Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vitreoretinal Degeneration Vitreoretinochoroidopathy Vitreoretinochoroidopathy Dominant Vitreoretinopathy, Neovascular Inflammatory Vitreous Detachment Vogt-Koyanagi-Harada Disease Von Hippel-Lindau Syndrome Wagner Syndrome Waldenstrom Macroglobulinemia Walker-Warburg Syndrome Wallerian Degeneration Weber Syndrome Weill-Marchesani Syndrome Werner Syndrome Wernicke Encephalopathy West Nile Virus Wiskott-Aldrich Syndrome Wolfram Syndrome Wolfram Syndrome 1 Wrinkles Wyburn Mason's Syndrome Xanthoma Disseminatum Xanthomatosis X-Linked Congenital Stationary Night Blindness Yellow Fever Yemenite Deaf-Blind Hypopigmentation Syndrome Zellweger Syndrome Zimmermann-Laband Syndrome Zimmermann-Laband Syndrome 1