Informaţii despre

Nume Leber Congenital Amaurosis 4
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary retinal dystrophy
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Leber Congenital Amaurosis 1; Leber Congenital Amaurosis 10; Leber Congenital Amaurosis 11; Leber Congenital Amaurosis 12; Leber Congenital Amaurosis 13; Leber Congenital Amaurosis 14; Leber Congenital Amaurosis 15; Leber Congenital Amaurosis 16; Leber Congenital Amaurosis 17; Leber Congenital Amaurosis 2; Leber Congenital Amaurosis 3; Leber Congenital Amaurosis 5; Leber Congenital Amaurosis 6; Leber Congenital Amaurosis 7; Leber Congenital Amaurosis 8; Leber Congenital Amaurosis 9

Vezi şi

Boli A-Z Abetalipoproteinemia Achromatopsia Achromatopsia 3 Acromegaly Adie Pupil Aging Albinism Alopecia Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Aniridia 1 Aniseikonia Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Disease Autosomal Recessive Non-Syndromic Intellectual Disability Bardet-Biedl Syndrome Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 8 Bietti Crystalline Corneoretinal Dystrophy Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blood Group--Ahonen Blood Group, I 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 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 Cervicitis Charles Bonnet Syndrome Cholestasis Chorioretinitis Choroideremia Choroiditis Chronic Granulomatous Disease Ciliary Dyskinesia, Primary, 1 Ciliopathy Coats Disease Common Variable Immunodeficiency Cone Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 7 Congenital Hepatic Fibrosis Congenital Stationary Night Blindness Congenital Toxoplasmosis Cryptorchidism, Unilateral or Bilateral Cutis Laxa Cutis Verticis Gyrata Dementia Dextrocardia Diabetes Mellitus Discoid Lupus Erythematosus Dysautonomia Enhanced S-Cone Syndrome Epilepsy Epithelial Recurrent Erosion Dystrophy Essential Iris Atrophy Esterase C Exfoliation Syndrome Exotropia 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 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 Hypophosphatasia Hypopituitarism Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration Hypoxia Ichthyosis Ichthyosis Prematurity Syndrome Intermediate Uveitis Interstitial Nephritis Intrahepatic Cholestasis Iridocyclitis Isolated Ectopia Lentis Keratoconus Late-Onset Retinal Degeneration Laurence-Moon Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 1 Leber Congenital Amaurosis 10 Leber Congenital Amaurosis 11 Leber Congenital Amaurosis 12 Leber Congenital Amaurosis 13 Leber Congenital Amaurosis 14 Leber Congenital Amaurosis 15 Leber Congenital Amaurosis 16 Leber Congenital Amaurosis 17 Leber Congenital Amaurosis 2 Leber Congenital Amaurosis 3 Leber Congenital Amaurosis 5 Leber Congenital Amaurosis 6 Leber Congenital Amaurosis 7 Leber Congenital Amaurosis 8 Leber Congenital Amaurosis 9 Leber Hereditary Optic Neuropathy Lens Subluxation Leukemia Lipid Metabolism Disorder Lissencephaly Lupus Erythematosus Macular Holes 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 Myopia Myotonia Myotonia Atrophica Myotonic Dystrophy Nephronophthisis Nervous System Disease Neurofibromatosis, Type Iv, of Riccardi Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neuropathy, Ataxia, and Retinitis Pigmentosa Neuroretinitis Nevus of Ota Night Blindness Nonsyndromic Retinitis Pigmentosa Occult Macular Dystrophy Oliver-Mcfarlane Syndrome Optic Disk Drusen Optic Nerve Hypoplasia, Bilateral Optic Pathway Glioma Osteochondrodysplasia Panic Disorder Papilledema Partial Central Choroid Dystrophy 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 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 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 3 Retinitis Pigmentosa 31 Retinitis Pigmentosa 33 Retinitis Pigmentosa 4 Retinitis Pigmentosa 45 Retinitis Pigmentosa 50 Retinitis Pigmentosa 6 Retinitis Pigmentosa 9 Retinoschisis 1, X-Linked, Juvenile Rheumatoid Arthritis Rhyns Syndrome Rud Syndrome Schizophrenia Scleromalacia Perforans Seizures, Benign Familial Neonatal, 1 Senior-Løken Syndrome Sensorineural Hearing Loss Sickle Cell Disease Situs Inversus Skeletal Dysplasias Small Cell Carcinoma Smith-Mccort Dysplasia 1 Spasticity Spastic Quadriplegia Spondylometaphyseal Dysplasia, Axial Stargardt Disease 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 Iia Uveitis Vici Syndrome 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