MeSH Treeview
Query OMIM entry list
602481
FHM2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Edema
Epilepsy
Epilepsy, Benign Neonatal
Seizures
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Migraine with Aura
Migraine without Aura
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Consciousness Disorders
Unconsciousness
Coma
Intellectual Disability
Paralysis
Hemiplegia
Seizures
Sensation Disorders
Vision Disorders
Photophobia
Eye Diseases
Vision Disorders
Photophobia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Epilepsy, Benign Neonatal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Recurrence
Signs and Symptoms
Body Temperature Changes
Fever
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Consciousness Disorders
Unconsciousness
Coma
Intellectual Disability
Paralysis
Hemiplegia
Seizures
Sensation Disorders
Vision Disorders
Photophobia
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