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Query OMIM entry list
602235
KCNQ2
POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 2
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsies, Partial
Epilepsy, Benign Neonatal
Epilepsy, Generalized
Seizures
Seizures, Febrile
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Myokymia
Paralysis
Quadriplegia
Seizures
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Long QT Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Long QT Syndrome
Infant, Newborn, Diseases
Epilepsy, Benign Neonatal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Arrhythmias, Cardiac
Long QT Syndrome
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Myokymia
Paralysis
Quadriplegia
Seizures
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