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ȘTIINȚE APLICATE
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Boli, Tulburări & Simptome
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XX Boli-semne, simptome
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Cataract
Informaţii despre
Nume
Cataract
Pagina Web
www.malacards.org
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
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