MeSH Treeview
Query OMIM entry list
601623
UBE3A
UBIQUITIN-PROTEIN LIGASE E3A
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Movement Disorders
Angelman Syndrome
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Rett Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Mental Retardation, X-Linked
Rett Syndrome
Prader-Willi Syndrome
Seizures
Male Urogenital Diseases
Genital Diseases, Male
Infertility
Infertility, Male
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
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Rett Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Rett Syndrome
Rett Syndrome
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosome Inversion
Translocation, Genetic
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Seizures
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