Informaţii despre

Nume Corneal Dystrophy
Pagina Web www.malacards.org
Clasificari ICD10 Hereditary corneal dystrophies
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Aging Al-Raqad Syndrome Amblyopia Aminoaciduria Amyloidosis Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Apparent Mineralocorticoid Excess Argyria Arthrochalasia Ehlers-Danlos Syndrome Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Autism Spectrum Disorder Autonomic Neuropathy Blood Group--Ahonen Blood Group, I System Cataract Choroiditis Corneal Degeneration Corneal Deposit Corneal Disease Corneal Dystrophy and Perceptive Deafness Corneal Dystrophy, Avellino Type Corneal Dystrophy, Congenital Stromal Corneal Dystrophy, Endothelial, X-Linked Corneal Dystrophy, Epithelial Basement Membrane Corneal Dystrophy, Fleck Corneal Dystrophy, Fuchs Endothelial, 2 Corneal Dystrophy, Fuchs Endothelial, 3 Corneal Dystrophy, Gelatinous Drop-Like Corneal Dystrophy, Groenouw Type I Corneal Dystrophy, Lattice Type I Corneal Dystrophy, Lattice Type Iiia Corneal Dystrophy, Lisch Epithelial Corneal Dystrophy, Meesmann Corneal Dystrophy, Posterior Amorphous Corneal Dystrophy, Posterior Polymorphous, 1 Corneal Dystrophy, Posterior Polymorphous, 2 Corneal Dystrophy, Posterior Polymorphous, 3 Corneal Dystrophy, Reis-Bucklers Type Corneal Dystrophy, Subepithelial Mucinous Corneal Dystrophy, Thiel-Behnke Type Corneal Edema Corneal Endothelial Dystrophy Corneal Granular Dystrophy Corneal Neovascularization Cutis Laxa, Autosomal Recessive, Type Iiia Endotheliitis Epithelial and Subepithelial Dystrophy Epithelial Basement Membrane Dystrophy Epithelial Recurrent Erosion Dystrophy Epithelial-Stromal Tgfbi Dystrophy Fabry Disease Fanconi Anemia, Complementation Group E Fuchs' Endothelial Dystrophy Helix Syndrome Hepatic Adenomas, Familial Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Ichthyosis Ichthyosis Prematurity Syndrome Juvenile Glaucoma Kearns-Sayre Syndrome Keloid Formation Keloids Keratoconus Lattice Corneal Dystrophy Lattice Corneal Dystrophy Type Ii Leukoencephalopathy, Hereditary Diffuse, with Spheroids Macular Dystrophy, Corneal Microcephaly Mousa Al Din Al Nassar Syndrome Mucopolysaccharidoses Myopia Myotonic Dystrophy Neuropathy Ocular Hypertension Pellucid Marginal Degeneration Polycystic Kidney Disease Polyneuropathy Posterior Cortical Atrophy Pre-Descemet Corneal Dystrophy Primary Cerebellar Degeneration Primary Congenital Glaucoma Punctate Epithelial Keratoconjunctivitis Recurrent Corneal Erosion Scheie Syndrome Schnyder Corneal Dystrophy Senile Cataract Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Spastic Ataxia Spasticity Spinocerebellar Degeneration Spondyloocular Syndrome Stromal Dystrophy Sveinsson Chorioretinal Atrophy
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