Informaţii despre

Nume Strabismus
Pagina Web www.malacards.org
Clasificari ICD10 Other specified strabismus; Strabismus, unspecified
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale

Vezi şi

Boli A-Z Abducens Nerve Disease Accommodative Esotropia Aging Albinism Albinism, Ocular, Type I 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 Amblyopia Amniotic Band Syndrome Anauxetic Dysplasia 1 Anencephaly Anhaptoglobinemia Aniridia 1 Aniseikonia Anisometropia Anorexia Nervosa 1 Apert Syndrome Aqueous Misdirection Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Asthma Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autosomal Recessive Stickler Syndrome Beare-Stevenson Cutis Gyrata Syndrome Blepharophimosis Blepharophimosis, Ptosis, and Epicanthus Inversus Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brachydactyly Brown Syndrome Cataract Cellulitis Cerebral Palsy Cerebral Visual Impairment Cerebritis Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Chorioretinitis Choroiditis Chromosomal Disease Chromosome 2q35 Duplication Syndrome Chromosome 8p23.1 Deletion Chronic Progressive External Ophthalmoplegia Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Nystagmus Congenital Ptosis Congenital Toxoplasmosis Cranial Nerve Disease Cranial Nerve Palsy Craniosynostosis Crouzon Syndrome Cutis Laxa, Autosomal Recessive, Type Iiia Cycloplegia Cyclotropia Deafness, Autosomal Dominant 28 Dextrocardia Distal Arthrogryposis Donnai-Barrow Syndrome Double Discordia Down Syndrome Duane-Radial Ray Syndrome Duane Retraction Syndrome Dysostosis Ectodermal Dysplasia Ectropion Ellis-Van Creveld Syndrome Endophthalmitis Enophthalmos Epicanthus Epidermoid Cysts Epilepsy Esotropia Exophthalmos Exotropia Facial Nerve Disease Fanconi Anemia, Complementation Group E Fibrosis of Extraocular Muscles, Congenital, 1 Fibrosis of Extraocular Muscles, Congenital, 2 Filamentary Keratitis Glioma Graves' Disease Headache Herpes Zoster Herpes Zoster Ophthalmicus Hypertropia Hypotonia Hypotrichosis Hypotropia Infantile Hypotonia Internuclear Ophthalmoplegia Intracranial Hypotension Iritis Ischemia Ischemic Optic Neuropathy Isolated Duane Retraction Syndrome Jackson-Weiss Syndrome Kearns-Sayre Syndrome Keratoconjunctivitis Keratoconus Keratopathy Lambert-Eaton Myasthenic Syndrome Laryngitis Laurence-Moon Syndrome Leukocoria Leukomalacia Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Luteoma Lyme Disease Machado-Joseph Disease Mechanical Strabismus Meningitis Microcephaly Moebius Syndrome Monofixation Syndrome Multiple Sclerosis Multisystemic Smooth Muscle Dysfunction Syndrome Myasthenia Gravis Myelomeningocele Myopia Myositis Myotonia Myotonia Congenita Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Ocular Dominance Ocular Motility Disease Ocular Neuromyotonia Oculocutaneous Albinism Optic Nerve Hypoplasia, Bilateral Optic Pathway Glioma Orbital Cellulitis Orbital Cyst Orbital Tenonitis Osseous Heteroplasia, Progressive Osteoglophonic Dysplasia Panophthalmitis Paralytic Squint Pathologic Nystagmus Periostitis Periventricular Leukomalacia Pineal Gland Cancer Plagiocephaly Poland Syndrome Polykaryocytosis Inducer Porencephaly Presbyopia Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 Ptosis Refractive Error Retinal Detachment Retinal Perforation Retinitis Retinoblastoma Rhombencephalosynapsis Schizophrenia Scleritis Scotoma Seizure Disorder Senile Cataract Situs Inversus Social Phobia Sotos Syndrome 1 Spasmus Nutans Spastic Ataxia, Charlevoix-Saguenay Type Spondyloocular Syndrome Spontaneous Intracranial Hypotension Stickler Syndrome Sturge-Weber Syndrome Suppression Amblyopia Synostosis Thoracolumbosacral Spina Bifida Aperta Thoracolumbosacral Spina Bifida Cystica Thrombosis Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Torticollis Total Spina Bifida Aperta Total Spina Bifida Cystica Toxoplasmoză Tuberculous Meningitis Tuberous Sclerosis Tukel Syndrome Upper Thoracic Spina Bifida Aperta Upper Thoracic Spina Bifida Cystica Vestibular Nystagmus Visual Epilepsy Visual Pathway Disease Weber Syndrome Williams-Beuren Syndrome Xerophthalmia X-Linked Infantile Nystagmus