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Query OMIM entry list
121200
EBN1
EPILEPSY, BENIGN NEONATAL, 1
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsies, Partial
Epilepsy, Benign Neonatal
Epilepsy, Generalized
Spasms, Infantile
Seizures
Seizures, Febrile
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Quadriplegia
Seizures
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Bone Marrow Diseases
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Chromosome Disorders
Infant, Newborn, Diseases
Epilepsy, Benign Neonatal
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Fanconi Anemia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Quadriplegia
Seizures
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