MeSH Treeview
Query OMIM entry list
608217
EBN3
EPILEPSY, BENIGN NEONATAL, 3
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High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsy, Benign Neonatal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Epilepsy, Benign Neonatal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosome Breakage
Chromosome Inversion
Database Center for Life Science
