Informaţii despre

Nume Retinitis Pigmentosa
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary retinal dystrophy
Clasificare anatomică Malacards Boli ale ochiului
Boli din aceeaşi familie Nonsyndromic 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 20; 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 30; Retinitis Pigmentosa 31; Retinitis Pigmentosa 32; Retinitis Pigmentosa 33; Retinitis Pigmentosa 34; Retinitis Pigmentosa 35; Retinitis Pigmentosa 36; Retinitis Pigmentosa 37; Retinitis Pigmentosa 38; Retinitis Pigmentosa 39; Retinitis Pigmentosa 4; Retinitis Pigmentosa 40; Retinitis Pigmentosa 41; Retinitis Pigmentosa 42; Retinitis Pigmentosa 43; Retinitis Pigmentosa 44; Retinitis Pigmentosa 45; Retinitis Pigmentosa 46; Retinitis Pigmentosa 47; Retinitis Pigmentosa 48; Retinitis Pigmentosa 49; Retinitis Pigmentosa 50; Retinitis Pigmentosa 51; Retinitis Pigmentosa 54; Retinitis Pigmentosa 55; Retinitis Pigmentosa 56; Retinitis Pigmentosa 57; Retinitis Pigmentosa 58; Retinitis Pigmentosa 59; Retinitis Pigmentosa 6; Retinitis Pigmentosa 60; Retinitis Pigmentosa 61; Retinitis Pigmentosa 62; Retinitis Pigmentosa 63; Retinitis Pigmentosa 66; Retinitis Pigmentosa 67; Retinitis Pigmentosa 68; Retinitis Pigmentosa 69; Retinitis Pigmentosa 7; Retinitis Pigmentosa 70; Retinitis Pigmentosa 71; Retinitis Pigmentosa 72; Retinitis Pigmentosa 73; Retinitis Pigmentosa 74; Retinitis Pigmentosa 75; Retinitis Pigmentosa 76; Retinitis Pigmentosa 77; Retinitis Pigmentosa 78; Retinitis Pigmentosa 79; Retinitis Pigmentosa 80; Retinitis Pigmentosa 81; Retinitis Pigmentosa 9; Retinitis Pigmentosa, Late-Adult Onset

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Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency Abetalipoproteinemia Achromatopsia Achromatopsia 3 Acromegaly Acute Zonal Occult Outer Retinopathy Aging Aland Island Eye Disease Albinism Alopecia Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Aniridia 1 Aniseikonia Anorexia Nervosa 1 Arterial Tortuosity Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Congenital Stationary Night Blindness Autosomal Dominant Disease Autosomal Recessive Non-Syndromic Intellectual Disability Bardet-Biedl Syndrome Bardet-Biedl Syndrome 1 Bardet-Biedl Syndrome 10 Bardet-Biedl Syndrome 11 Bardet-Biedl Syndrome 12 Bardet-Biedl Syndrome 13 Bardet-Biedl Syndrome 14 Bardet-Biedl Syndrome 15 Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 3 Bardet-Biedl Syndrome 4 Bardet-Biedl Syndrome 6 Bardet-Biedl Syndrome 8 Bietti Crystalline Corneoretinal Dystrophy Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blood Group--Ahonen Blood Group, I System Blue Cone Monochromacy 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 Brachydactyly Brachymorphism-Onychodysplasia-Dysphalangism Syndrome Branch Retinal Artery Occlusion Bronchiectasis Cataract Central Nervous System Disease Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebellar Degeneration Cerebellar Hypoplasia Ceroid Lipofuscinosis, Neuronal, 3 Cerulean Cataract Cervicitis Charles Bonnet Syndrome Cholestasis Chorioretinitis Choroidal Dystrophy, Central Areolar, 1 Choroideremia Choroiditis Chronic Granulomatous Disease Ciliary Dyskinesia, Primary, 1 Ciliopathy Coats Disease Color Blindness Color Vision Deficiency Common Variable Immunodeficiency Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 3 Cone-Rod Dystrophy 6 Cone-Rod Dystrophy 7 Cone-Rod Dystrophy and Hearing Loss Congenital Hepatic Fibrosis Congenital Stationary Night Blindness Congenital Toxoplasmosis Corneal Dystrophy, Thiel-Behnke Type Cryptorchidism, Unilateral or Bilateral Cutis Laxa Cutis Verticis Gyrata Cystic Kidney Disease Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 23 Deafness Enamel Hypoplasia Nail Defects Deafness, X-Linked 2 Degeneration of Macula and Posterior Pole Dementia Dextrocardia Dfnb1 Diabetes Mellitus Discoid Lupus Erythematosus Dysautonomia Enhanced S-Cone Syndrome Epilepsy Epithelial Recurrent Erosion Dystrophy Essential Iris Atrophy Esterase C Exfoliation Syndrome Exotropia Eye Degenerative Disease Familial Paroxysmal Nonkinesigenic Dyskinesia Fanconi Syndrome Focal Segmental Glomerulosclerosis Foster-Kennedy Syndrome Fuchs' Heterochromic Uveitis Fundus Albipunctatus Fundus Dystrophy Glioma Goldmann-Favre Syndrome Growth Hormone Deficiency Gyrate Atrophy of Choroid and Retina Helix Syndrome Hematopoietic Stem Cell Transplantation Hemifacial Atrophy, Progressive Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hereditary Choroidal Atrophy Hereditary Night Blindness Hereditary Retinal Dystrophy Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoaldosteronism Hypoglycemia Hypogonadism Hypoparathyroidism-Retardation-Dysmorphism Syndrome Hypophosphatasia Hypopituitarism Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration Hypoxia Ichthyosis Ichthyosis Prematurity Syndrome Intermediate Uveitis Interstitial Nephritis Intrahepatic Cholestasis Iridocyclitis Isolated Ectopia Lentis Joubert Syndrome 1 Keratoconus Keratomalacia Late-Onset Retinal Degeneration Laurence-Moon Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 10 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 14 Leber Congenital Amaurosis 3 Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 5 Leber Congenital Amaurosis 9 Leber Hereditary Optic Neuropathy Lens Subluxation Leukemia Lipid Metabolism Disorder Lissencephaly Lupus Erythematosus Macular Degeneration, Age-Related, 1 Macular Dystrophy, Dominant Cystoid Macular Dystrophy, Vitelliform, 3 Macular Holes Macular Retinal Edema Marfan Syndrome Mckusick-Kaufman Syndrome Mcleod Syndrome Mevalonic Aciduria Microcephaly Miller-Dieker Lissencephaly Syndrome Miyoshi Muscular Dystrophy 1 Mucopolysaccharidosis Iii Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis, Type Iiic Muscular Dystrophy Muscular Dystrophy, Duchenne Type Myopia Myotonia Myotonia Atrophica Myotonic Dystrophy Nephronophthisis Nephronophthisis 1 Nephronophthisis 16 Nephronophthisis 2 Nephronophthisis 3 Nervous System Disease Neurofibromatosis, Type Iv, of Riccardi Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neuropathy, Ataxia, and Retinitis Pigmentosa Neuroretinitis Nevus of Ota Night Blindness Night Blindness, Congenital Stationary, Type 2a Nonsyndromic Retinitis Pigmentosa Occult Macular Dystrophy Oliver-Mcfarlane Syndrome Optic Disk Drusen Optic Nerve Hypoplasia, Bilateral Optic Pathway Glioma Orofaciodigital Syndrome I Osteochondrodysplasia Panic Disorder Papilledema Paroxysmal Nonkinesigenic Dyskinesia 1 Partial Central Choroid Dystrophy Peripheral Retinal Degeneration Peutz-Jeghers Syndrome Phelan-Mcdermid Syndrome Phimosis Pigmented Paravenous Chorioretinal Atrophy Polycystic Kidney Disease Polydactyly Polyneuropathy Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Posterior Column Ataxia Posterior Column Ataxia with Retinitis Pigmentosa Posterior Polar Cataract Premature Chromatid Separation Trait Primary Angle-Closure Glaucoma Primary Ciliary Dyskinesia Prolonged Electroretinal Response Suppression Pseudohypoparathyroidism Pseudoxanthoma Elasticum Pulmonary Hemosiderosis Quadriplegia Radin Blood Group Antigen Red-Green Color Blindness Refsum Disease, Classic Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Artery Occlusion Retinal Cone Dystrophy 1 Retinal Degeneration Retinal Detachment Retinal Disease Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis 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 32 Retinitis Pigmentosa 33 Retinitis Pigmentosa 34 Retinitis Pigmentosa 35 Retinitis Pigmentosa 4 Retinitis Pigmentosa 45 Retinitis Pigmentosa 50 Retinitis Pigmentosa 6 Retinitis Pigmentosa 63 Retinitis Pigmentosa 66 Retinitis Pigmentosa 9 Retinitis Pigmentosa, Y-Linked Retinopathy, Pericentral Pigmentary, Autosomal Recessive Retinoschisis 1, X-Linked, Juvenile Rheumatoid Arthritis Rhyns Syndrome Rud Syndrome Schizophrenia Scleromalacia Perforans Seizures, Benign Familial Neonatal, 1 Senior-Løken Syndrome Senior-Loken Syndrome 1 Sensorineural Hearing Loss Severe Early-Childhood-Onset Retinal Dystrophy Sickle Cell Disease Situs Inversus Skeletal Dysplasias Small Cell Carcinoma Smith-Mccort Dysplasia 1 Spasticity Spastic Quadriplegia Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spondylometaphyseal Dysplasia, Axial Stargardt Disease Stargardt Disease 1 Stargardt Macular Degeneration Steatorrhea Sturge-Weber Syndrome Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxoplasmoză Trichomegaly Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina Trnt1 Deficiency 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 Iia Usher Syndrome, Type Iic Usher Syndrome, Type Iid Usher Syndrome, Type Iiia Uveitis Vici Syndrome Vitelliform Macular Dystrophy Vitreous Detachment Weber Syndrome Weill-Marchesani Syndrome X-Linked Congenital Stationary Night Blindness Yemenite Deaf-Blind Hypopigmentation Syndrome Zimmermann-Laband Syndrome Zimmermann-Laband Syndrome 1