Informaţii despre

Nume Myopia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Myopia
Clasificare anatomică Malacards Boli ale ochiului
Boli din aceeaşi familie Myopia 10; Myopia 11, Autosomal Dominant; Myopia 12, Autosomal Dominant; Myopia 14; Myopia 15, Autosomal Dominant; Myopia 16, Autosomal Dominant; Myopia 17, Autosomal Dominant; Myopia 18, Autosomal Recessive; Myopia 19, Autosomal Dominant; Myopia 2, Autosomal Dominant; Myopia 20, Autosomal Dominant; Myopia 21, Autosomal Dominant; Myopia 22, Autosomal Dominant; Myopia 23, Autosomal Recessive; Myopia 24, Autosomal Dominant; Myopia 25, Autosomal Dominant; Myopia 3, Autosomal Dominant; Myopia 5, Autosomal Dominant; Myopia 6; Myopia 7; Myopia 8; Myopia 9

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Boli A-Z 48,xxyy Syndrome 49,xxxxy Syndrome Acanthamoeba Keratitis Accommodative Esotropia Accommodative Spasm Achondrogenesis, Type Ii Achromatopsia Acute Closed-Angle Glaucoma Aging Allergic Conjunctivitis Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Angioid Streaks Aniridia 1 Aniseikonia Anisometropia Anorexia Nervosa 1 Aplasia Cutis Congenita Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction Aqueous Misdirection Arachnoid Cysts Arachnoiditis Arcus Corneae Arthrochalasia Ehlers-Danlos Syndrome Asthenopia Astigmatism Ataxia and Polyneuropathy, Adult-Onset Autosomal Dominant Congenital Stationary Night Blindness Autosomal Recessive Congenital Stationary Night Blindness Autosomal Recessive Stickler Syndrome Baraitser-Winter Syndrome 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Cone Monochromacy Bohring-Opitz Syndrome Bornholm Eye Disease Bullous Keratopathy Cataract Cataract 40 Cataract, Total Congenital Central Serous Chorioretinopathy Chorioretinitis Choroideremia Choroiditis Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Cohen Syndrome Collagen Disease Coloboma of Iris Color Blindness Colorblindness, Partial, Protan Series Color Vision Deficiency Cone Dystrophy Congenital Myasthenic Syndrome Congenital Ptosis Congenital Stationary Night Blindness Conjunctivitis Conversion Disorder Corneal Dystrophy Corneal Dystrophy, Congenital Stromal Corneal Ectasia Corneal Ulcer Cornea Plana Cutis Laxa Cycloplegia Deafness and Myopia Degenerative Myopia Diabetes Mellitus Down Syndrome Dry Eye Syndrome Dupuytren Contracture Dwarfism Endotheliitis Erythema Multiforme Esotropia Exfoliation Syndrome Exophthalmos Exotropia Exudative Vitreoretinopathy Fanconi Anemia, Complementation Group E Fundus Albipunctatus Galactose Epimerase Deficiency Glioma Gyrate Atrophy of Choroid and Retina Haim-Munk Syndrome Headache Hepatic Adenomas, Familial Hereditary Night Blindness Histoplasmosis Holt-Oram Syndrome Hydrophthalmos Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypopyon Hypotonia Hypotropia Idiopathic Hypercalciuria Immunoglobulin E Concentration, Serum Iritis Irregular Astigmatism Isolated Ectopia Lentis Juvenile Glaucoma Keratoconjunctivitis Keratoconus Keratopathy Kniest Dysplasia Leber Congenital Amaurosis 4 Lens Subluxation Leukomalacia Limbal Stem Cell Deficiency Lmna-Related Cardiocutaneous Progeria Syndrome Loeys-Dietz Syndrome Lupus Erythematosus Macroglossia Macular Holes Malignant Spiradenoma Marshall Syndrome Meckel Syndrome, Type 1 Melanoma Microphthalmia Migraine with or Without Aura 1 Miyoshi Muscular Dystrophy 1 Mousa Al Din Al Nassar Syndrome Multifocal Choroiditis Multiple Epiphyseal Dysplasia Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly Myopathy Myopia 10 Myopia 11, Autosomal Dominant Myopia 12, Autosomal Dominant Myopia 13, X-Linked Myopia 14 Myopia 15, Autosomal Dominant Myopia 16, Autosomal Dominant Myopia 17, Autosomal Dominant Myopia 18, Autosomal Recessive Myopia 1, X-Linked Myopia 2, Autosomal Dominant Myopia 3, Autosomal Dominant Myopia 5, Autosomal Dominant Myopia 6 Myopia 7 Myopia 8 Myopia 9 Neonatal Marfan Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuronitis Night Blindness Night Blindness, Congenital Stationary, Type 1a Night Blindness, Congenital Stationary, Type 1b Night Blindness, Congenital Stationary, Type 1e Night Blindness, Congenital Stationary, Type 2a Ocular Hypertension Open-Angle Glaucoma Ophthalmoplegia, External, and Myopia Opitz-Kaveggia Syndrome Optic Nerve Glioma Optic Nerve Hypoplasia, Bilateral Orbital Tenonitis Otospondylomegaepiphyseal Dysplasia Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive Pachygyria Pellucid Marginal Degeneration Pemphigus Pemphigus Vulgaris Peripheral Retinal Degeneration Periventricular Leukomalacia Persistent Hyperplastic Primary Vitreous Peutz-Jeghers Syndrome Plexiform Neurofibroma Posterior Polar Cataract Presbyopia Presynaptic Congenital Myasthenic Syndromes Primary Angle-Closure Glaucoma Primary Congenital Glaucoma Prolidase Deficiency Pseudoachondroplasia Pseudoxanthoma Elasticum Ptosis Ptosis, Hereditary Congenital 2 Rare Isolated Myopia Red-Green Color Blindness Refractive Error Retinal Degeneration Retinal Detachment Retinal Perforation Retinal Telangiectasia Retinitis Retinitis Pigmentosa Rheumatic Disease Scleral Staphyloma Scleritis Scoliosis Scotoma Senile Cataract Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sorsby Fundus Dystrophy Spastic Ataxia Spasticity Spinal Stenosis Stickler Syndrome Strabismus Stromal Dystrophy Sturge-Weber Syndrome Suppressor of Tumorigenicity 3 Systemic Lupus Erythematosus Three M Syndrome 1 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Traumatic Glaucoma Triple X Syndrome Tukel Syndrome Vitreoretinal Degeneration Vitreous Detachment Vitreous Disease Vogt-Koyanagi-Harada Disease Weber Syndrome Weill-Marchesani Syndrome X-Linked Congenital Stationary Night Blindness