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Query OMIM entry list
607745
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SEIZURES, BENIGN FAMILIAL NEONATAL-INFANTILE
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsy, Benign Neonatal
Seizures
Neurologic Manifestations
Seizures
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Infant, Newborn, Diseases
Epilepsy, Benign Neonatal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Signs and Symptoms
Neurologic Manifestations
Seizures
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