MeSH Treeview
Query OMIM entry list
600497
PRKAA2
PROTEIN KINASE, AMP-ACTIVATED, CATALYTIC, ALPHA-2
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Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Body Weight
Signs and Symptoms, Respiratory
Anoxia
Database Center for Life Science
