MeSH Treeview
Query OMIM entry list
162151
PCSK2
PROPROTEIN CONVERTASE, SUBTILISIN/KEXIN-TYPE, 2
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Database Center for Life Science
