MeSH Treeview
Query OMIM entry list
605837
HERC2
HECT DOMAIN AND RCC1-LIKE DOMAIN 2
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Nervous System Diseases
Central Nervous System Diseases
Movement Disorders
Angelman Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Neuromuscular Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Angelman Syndrome
Prader-Willi Syndrome
Chromosome Disorders
Angelman Syndrome
Prader-Willi Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Angelman Syndrome
Prader-Willi Syndrome
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Animal Diseases
Disease Models, Animal
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