Informaţii despre

Nume Cataract
Pagina Web
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Cataract in other diseases classified elsewhere; Cataract, unspecified; Other specified cataract
Clasificare anatomică Malacards Boli ale ochiului; Boli bucale; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Cataract 1, Multiple Types; Cataract 10, Multiple Types; Cataract 11, Multiple Types; Cataract 12, Multiple Types; Cataract 14, Multiple Types; Cataract 15, Multiple Types; Cataract 16, Multiple Types; Cataract 17, Multiple Types; Cataract 18; Cataract 19, Multiple Types; Cataract 2, Multiple Types; Cataract 20, Multiple Types; Cataract 21, Multiple Types; Cataract 22, Multiple Types; Cataract 23, Multiple Types; Cataract 24; Cataract 25; Cataract 26, Multiple Types; Cataract 27; Cataract 28; Cataract 29; Cataract 3, Multiple Types; Cataract 30; Cataract 30, Multiple Types; Cataract 31, Multiple Types; Cataract 32, Multiple Types; Cataract 33; Cataract 33, Multiple Types; Cataract 34, Multiple Types; Cataract 35; Cataract 36; Cataract 37; Cataract 38; Cataract 39, Multiple Types; Cataract 4, Multiple Types; Cataract 40; Cataract 41; Cataract 42; Cataract 43; Cataract 44; Cataract 45; Cataract 46, Juvenile-Onset; Cataract 47; Cataract 5, Multiple Types; Cataract 6, Multiple Types; Cataract 7; Cataract 8, Multiple Types; Cataract 9, Multiple Types; Cataract Congenital Autosomal Dominant; Cataract, Total Congenital

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria 47,xyy Ablepharon-Macrostomia Syndrome Acanthamoeba Keratitis Accommodative Esotropia Acoustic Neuroma Acquired Immunodeficiency Syndrome Acrodermatitis Acute Endophthalmitis Adams-Oliver Syndrome Adenoid Hypertrophy Adenoiditis Adrenomyodystrophy Adult T-Cell Leukemia Aging Albinism Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Alopecia 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 Aminoaciduria Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aniridia 1 Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract Aniseikonia Anisometropia Anorexia Nervosa 1 Anterior Segment Dysgenesis 1 Anterior Segment Dysgenesis 2 Anterior Uveitis Aortitis Apparent Mineralocorticoid Excess Aqueous Misdirection Arterial Tortuosity Syndrome Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Arthropathy Aspergillosis Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Microcephaly-Cataract Syndrome Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Atypical Teratoid Rhabdoid Tumor Autoimmune Hypoparathyroidism Axenfeld-Rieger Syndrome Axonal Neuropathy Ayme-Gripp Syndrome Azoospermia Bacteriuria Bannayan-Riley-Ruvalcaba Syndrome Beta-Thalassemia Bilateral Retinoblastoma Bleeding Disorder, Platelet-Type, 11 Blepharitis Blepharophimosis Blood Group--Ahonen Blood Group, Dombrock System 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation Brachydactyly Branchiootic Syndrome 1 Branchiootorenal Syndrome Bronchopulmonary Dysplasia Bullous Keratopathy Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Cardiomyopathy Cataract Hip Spine Disease Cataract 10, Multiple Types Cataract 11, Multiple Types Cataract 14, Multiple Types Cataract 16, Multiple Types Cataract 1, Multiple Types Cataract 24 Cataract 25 Cataract 27 Cataract 28 Cataract 29 Cataract 2, Multiple Types Cataract 30 Cataract 30, Multiple Types Cataract 32, Multiple Types Cataract 35 Cataract 37 Cataract 40 Cataract 44 Cataract 4, Multiple Types Cataract 5, Multiple Types Cataract 6, Multiple Types Cataract 7 Cataract 9, Multiple Types Cataract, Ataxia, Short Stature, and Mental Retardation Cataract-Glaucoma Cataract Microcornea Syndrome Cavernous Sinus Thrombosis Cdkl5-Related Disorder Cellulitis Centronuclear Myopathy Cerebellar Hypoplasia Cerebritis Cerebrotendinous Xanthomatosis Cerulean Cataract Cervicitis Charcot-Marie-Tooth Disease Charge Syndrome Choanal Atresia, Posterior Chondrodysplasia Punctata Syndrome Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroideremia Choroiditis Chromoblastomycosis Chromosomal Triplication Chromosome 10q Deletion Chromosome 12p Duplication Chromosome 15q11.2 Deletion Syndrome Chronic Closed-Angle Glaucoma Chronic Endophthalmitis Cicatricial Pemphigoid Cluster Headache Coats Disease Cockayne Syndrome Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone Dystrophy Congenital Aphakia Congenital Cataracts, Facial Dysmorphism, and Neuropathy Congenital Herpes Simplex Congenital Rubella Congenital Toxoplasmosis Conjunctivitis Conjunctivochalasis Constricting Bands, Congenital Corneal Degeneration Corneal Deposit Corneal Disease Corneal Dystrophy Corneal Ectasia Corneal Edema Corneal Ulcer Costello Syndrome Coxa Vara Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniofacial Microsomia Craniosynostosis Creutzfeldt-Jakob Disease Cri-Du-Chat Syndrome Cutis Laxa Cutis Laxa, Autosomal Recessive, Type Iiia Cutis Marmorata Telangiectatica Congenita Cutis Verticis Gyrata Cycloplegia Cystic Fibrosis Cystinosis Cytomegalovirus Retinitis Dandy-Walker Complex Dementia Dent Disease 1 Dermatitis Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Cataract Diabetic Macular Edema Diabetic Neuropathy Diarrhea Diffuse Mesangial Sclerosis Dilated Cardiomyopathy Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation Disuse Amblyopia Down Syndrome Dry Eye Syndrome Duane Retraction Syndrome 1 Dubowitz Syndrome Dwarfism Dyskeratosis Congenita Dysostosis Dysphagia Early-Onset Glaucoma Early-Onset Nuclear Cataract Early-Onset Posterior Subcapsular Cataract Ectodermal Dysplasia Ectropion Eczema Herpeticum Edict Syndrome Encephalitis Encephalitozoonosis Encephalomyopathy Encephalopathy Endocardial Fibroelastosis Endophthalmitis Endotheliitis Enteropathica Entropion Epidermolysis Bullosa Epilepsy Epimerase Deficiency Galactosemia Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Esotropia Exfoliation Syndrome Exophthalmos Exotropia Exposure Keratitis Exudative Vitreoretinopathy Eye Accommodation Disease Factor Xi Deficiency Fanconi Anemia, Complementation Group E Fanconi-Bickel Syndrome Fibrocalculous Pancreatopathy Filamentary Keratitis Foster-Kennedy Syndrome Fuchs' Endothelial Dystrophy Fuchs' Heterochromic Uveitis Galactokinase Deficiency Galactose Epimerase Deficiency Galactosemia Galactosialidosis Gardner-Diamond Syndrome Gastroesophageal Reflux Giant Papillary Conjunctivitis Gigantism Glaucoma, Hereditary Glaucoma, Normal Tension Glaucoma, Primary Open Angle Glioma Glucose Intolerance Glucosephosphate Dehydrogenase Deficiency Glycogen Storage Disease Ii Gonadoblastoma Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy Growth Hormone Deficiency Gyrate Atrophy of Choroid and Retina Hallermann-Streiff Syndrome Hansen's Disease Hantavirus Pulmonary Syndrome Headache Hemochromatosis, Neonatal Hemochromatosis, Type 4 Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hereditary Spastic Paraplegia Hereditary Wilms' Tumor Herpes Simplex Herpes Simplex Virus Keratitis Herpes Zoster Herpes Zoster Ophthalmicus Heterochromia Iridis Homocystinuria Horns in Sheep Hydrocephalus Hydrocephalus, Endocardial Fibroelastosis, and Cataracts Hydrophthalmos Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperferritinemia with or Without Cataract Hyperglycemia Hyperglycinuria Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertropia Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomelanosis of Ito Hypomelanotic Disorder Hypoparathyroidism Hypopyon Hypotonia Hypotrichosis Ichthyosis Immature Cataract Infertility Intermediate Uveitis Interstitial Keratitis Intracranial Hypertension Iridocyclitis Iris Pattern Iritis Irregular Astigmatism Ischemia Ischemic Optic Neuropathy Isolated Ectopia Lentis Isolated Growth Hormone Deficiency, Type Ia Juvenile Rheumatoid Arthritis Juvenile Xanthogranuloma Keratitis, Hereditary Keratoconjunctivitis Keratoconjunctivitis Sicca Keratoconus Keratoconus Posticus Circumscriptus Keratomalacia Keratopathy Kniest Dysplasia Knobloch Syndrome Lacrimal Duct Defect Lactic Acidosis Lactose Intolerance Laryngitis Late-Onset Retinal Degeneration Lathosterolosis Lattice Corneal Dystrophy Lattice Corneal Dystrophy Type Ii Laurin-Sandrow Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 4 Leber Congenital Amaurosis 5 Leigh Syndrome Leiomyomatosis Lens Disease Lens Subluxation Leukemia Leukodystrophy Leukodystrophy, Hypomyelinating, 5 Limbal Stem Cell Deficiency Lipodystrophy Lissencephaly Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lowe Oculocerebrorenal Syndrome Lubinsky Syndrome Lymphadenitis Lymphoma Macular Holes Major Affective Disorder 2 Mal De Meleda Male Infertility Malignant Spiradenoma Marden-Walker Syndrome Marfan Syndrome Marinesco-Sjogren Syndrome Mast Cell Activation Syndrome Mature Cataract Meckel Syndrome, Type 1 Medulloepithelioma Megalocornea Melanoma Meningitis Meningococcal Meningitis Mevalonic Aciduria Microcephalic Primordial Dwarfism, Toriello Type Microcephaly Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance Microcephaly Microcornea Syndrome Seemanova Type Microphthalmia Microphthalmia, Isolated 2 Microphthalmia, Isolated, with Cataract 1 Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Monilethrix Monofixation Syndrome Morgagni Cataract Morning Glory Syndrome Morquio Syndrome Mousa Al Din Al Nassar Syndrome Mucopolysaccharidosis Iv Mucopolysaccharidosis-Plus Syndrome Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Epiphyseal Dysplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multisystemic Smooth Muscle Dysfunction Syndrome Muscular Atrophy Muscular Dystrophy Myasthenia Gravis Mycobacterium Abscessus Mycobacterium Chelonae Myh-9 Related Disease Myhre Syndrome Myofibrillar Myopathy Myopathy Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay Myopia Myotonia Myotonic Dystrophy Nance-Horan Syndrome Neonatal Jaundice Neovascular Glaucoma Nephrocalcinosis Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neurodermatitis Neurofibromatosis, Type Iv, of Riccardi Neuroma Neuromuscular Disease Neuromyelitis Optica Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neurotrophic Keratopathy Neutropenia Nevus of Ota Nievergelt Syndrome Nipples, Supernumerary Nonarteritic Anterior Ischemic Optic Neuropathy Nuclear Senile Cataract Ocular Cicatricial Pemphigoid Ocular Hypertension Ocular Hypotension Ocular Melanoma Ocular Toxoplasmosis Oculoauricular Syndrome Oculocutaneous Albinism Oliver Syndrome Olivopontocerebellar Atrophy Open-Angle Glaucoma Ophthalmomyiasis Optic Atrophy 3, Autosomal Dominant Optic Disk Drusen Optic Nerve Hypoplasia, Bilateral Optic Papillitis Orbital Cellulitis Orbital Tenonitis Orbital Varix Pancreatitis Panophthalmitis Panuveitis Papillary Conjunctivitis Papilledema Paraplegia Parkinsonism with Spasticity, X-Linked Pars Planitis Pearson Marrow-Pancreas Syndrome Pellagra Pellucid Marginal Degeneration Penicillin Allergy Pericarditis Peritonitis Peroxisomal Biogenesis Disorders Peroxisome Biogenesis Disorder 14b Peroxisome Disorders Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Peters-Plus Syndrome Phacoanaphylactic Uveitis Phacolytic Glaucoma Phimosis Pinguecula Podoconiosis Polyarteritis Nodosa Polyhydramnios Polymicrogyria Polyneuropathy Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes Porencephaly Posterior Polar Cataract Posterior Uveitis Presbyopia Primary Angle-Closure Glaucoma Primary Congenital Glaucoma Prostatitis Pseudohypoparathyroidism Pten Hamartoma Tumor Syndrome Ptosis Pulmonary Edema Pulsating Exophthalmos Pyoderma Pyoderma Gangrenosum Pyridoxine Deficiency Pyridoxine Deficiency Anemia Refractive Error Regular Astigmatism Renal Dysplasia Renal Glucosuria Renal Tubular Acidosis Renpenning Syndrome 1 Reticulum Cell Sarcoma Retinal Aplasia Retinal Artery Occlusion Retinal Degeneration Retinal Detachment Retinal Disease Retinal Ischemia Retinal Perforation Retinal Vasculitis Retinitis Retinitis Pigmentosa Retinoblastoma Rheumatoid Arthritis Rhizomelic Chondrodysplasia Punctata Ring Chromosome 16 Rothmund-Thomson Syndrome Rubella Rubeosis Iridis Ruvalcaba Syndrome Sarcoma Schaap Taylor Baraitser Syndrome Schizencephaly Scleritis Sclerosing Keratitis Scoliosis Scotoma Seizure Disorder Sengers Syndrome Senile Cataract Senior-Løken Syndrome Sensorineural Hearing Loss Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sick Sinus Syndrome Sjogren Syndrome Skin Disease Smith-Lemli-Opitz Syndrome Sotos Syndrome 1 Spastic Ataxia Spastic Entropion Spasticity Spastic Paraparesis Spastic Paraplegia 9 Spinal Muscular Atrophy Spondyloepimetaphyseal Dysplasia, Sponastrime Type Spondyloocular Syndrome Squamous Cell Carcinoma Stenotrophomonas Maltophilia Infection Steroid-Induced Glaucoma Stickler Syndrome St. Louis Encephalitis Strabismus Sturge-Weber Syndrome Supernumerary Nostril Sveinsson Chorioretinal Atrophy Sympathetic Ophthalmia Tardive Dyskinesia T Cell Deficiency T-Cell Leukemia Teratoma Tetanic Cataract Thalassemia Three M Syndrome 1 Thrombocytopenia Thrombocytopenia 1 Thrombosis Thyroiditis Tooth Disease Toxocariasis Toxoplasmoză Tracheoesophageal Fistula Trachoma Transient Retinal Arterial Occlusion Trichomegaly Trisomy 17 Mosaicism Trnt1 Deficiency Turner Syndrome Usher Syndrome Uveitis Vascular Disease Vasculitis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vitreoretinal Degeneration Vitreoretinochoroidopathy Vitreous Detachment Vogt-Koyanagi-Harada Disease Wagner Syndrome Walker-Warburg Syndrome Warburg Micro Syndrome Warburg Micro Syndrome 1 Weber Syndrome Werner Syndrome Wilms Tumor 6 Wilson Disease Wolfram Syndrome Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Yemenite Deaf-Blind Hypopigmentation Syndrome Zellweger Spectrum Disorder Zimmermann-Laband Syndrome Zimmermann-Laband Syndrome 1