MeSH Treeview
Query OMIM entry list
607541
CDA
CORNEAL DYSTROPHY, AVELLINO TYPE
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Nervous System Diseases
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Corneal Opacity
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Vision Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Recurrence
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
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