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Query OMIM entry list
122200
CDL1
CORNEAL DYSTROPHY, LATTICE TYPE I
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Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Ocular Hypertension
Glaucoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Nutritional and Metabolic Diseases
Metabolic Diseases
Proteostasis Deficiencies
Amyloidosis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Recurrence
Database Center for Life Science
