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Searching Condition for "Epilepsy" · search everything instead
60 results
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Absence EpilepsyConditionTopicsyndrome ICD-10G40.7 MeSHD004832 HERBHBDIS000961disease · Nervous System Diseases
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Absence Seizure DisorderConditionTopicsyndrome MeSHD004832 HERBHBDIS027469disease · Nervous System Diseases
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Action Myoclonus-Renal Failure SyndromeConditionTopicsyndrome OMIM254900 MeSHD020191 HERBHBDIS011456disease · Nervous System Diseases
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Adult Neuronal Ceroid LipofuscinosisConditionTopicsyndrome OMIM204300 MeSHD009472 HERBHBDIS001633disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
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Akinetic Petit MalConditionTopicsyndrome MeSHD004832 HERBHBDIS000094disease · Nervous System Diseases
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Amish Infantile Epilepsy SyndromeConditionTopicsyndrome OMIM609056 MeSHC563799 HERBHBDIS015489disease · Nervous System Diseases
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Amygdalo-Hippocampal EpilepsyConditionTopicsyndrome MeSHD004828 HERBHBDIS028483disease · Nervous System Diseases
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Arnold-Chiari Syndrome, Type IvConditionTopicsyndrome HERBHBDIS029211disease
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Atypical Benign Partial EpilepsyConditionTopicsyndrome HERBHBDIS012648disease
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Atypical Inclusion-Body DiseaseConditionTopicsyndrome MeSHD020191 HERBHBDIS011453disease · Nervous System Diseases
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AuraConditionTopicphenotype MeSHD004827 HERBHBDIS005039phenotype · Nervous System Diseases
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Autosomal Dominant Lateral Temporal Lobe EpilepsyConditionTopicsyndrome OMIM600512 MeSHC537297 HERBHBDIS015644disease · Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
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Autosomal Dominant Nocturnal Frontal Lobe EpilepsyConditionTopicsyndrome MeSHC579932 HERBHBDIS022022disease · Nervous System Diseases
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Autosomal Recessive Cerebellar Ataxia, Epilepsy, Intellectual Disability Syndrome Due To Wwox DeficiencyConditionTopicsyndrome HERBHBDIS028159disease · Mental Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Behavior and Behavior Mechanisms; Pathological Conditions, Signs and Symptoms
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Awakening EpilepsyConditionTopicsyndrome MeSHD004827 HERBHBDIS011161disease · Nervous System Diseases
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Benign Adult Familial Myoclonic EpilepsyConditionTopicsyndrome HERBHBDIS025892disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
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Benign Familial Mesial Temporal Lobe EpilepsyConditionTopicsyndrome HERBHBDIS028143disease · Nervous System Diseases
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Benign Focal Epilepsy, ChildhoodConditionTopicsyndrome MeSHD004828 HERBHBDIS028376disease · Nervous System Diseases
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Benign Infantile Myoclonic EpilepsyConditionTopicsyndrome MeSHD004831 HERBHBDIS011165disease · Nervous System Diseases
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Benign Neonatal EpilepsyConditionTopicsyndrome MeSHD020936 HERBHBDIS006513disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Benign Neonatal Epilepsy, NonfamilialConditionTopicsyndrome MeSHD020936 HERBHBDIS008699disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Benign Occipital EpilepsyConditionTopicsyndrome OMIM132090 MeSHD004828 HERBHBDIS028896disease · Nervous System Diseases
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Benign Rolandic EpilepsyConditionTopicsyndrome OMIM117100 MeSHD019305 HERBHBDIS019137disease · Nervous System Diseases
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Biotin-Responsive EncephalopathyConditionTopicsyndrome MeSHD020191 HERBHBDIS011457disease · Nervous System Diseases
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Ceroid Lipofuscinosis, Neuronal, 8ConditionTopicsyndrome OMIM600143 MeSHC537952 HERBHBDIS015690disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
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Childhood Absence EpilepsyConditionTopicsyndrome MeSHD004832 HERBHBDIS025983disease · Nervous System Diseases
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Childhood Benign Occipital EpilepsyConditionTopicsyndrome MeSHD004828 HERBHBDIS028482disease · Nervous System Diseases
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Continuous Spike And Waves During Slow SleepConditionTopicsyndrome OMIM245570 HPOHP:0031491 HERBHBDIS022218disease
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Convulsions, Benign Familial Infantile, 1ConditionTopicsyndrome OMIM601764 MeSHD020936 HERBHBDIS027303disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Convulsions, Benign Familial Infantile, 4ConditionTopicsyndrome OMIM612627 MeSHC567231 HERBHBDIS019372disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Cortical Dysplasia With Focal Epilepsy SyndromeConditionTopicsyndrome OMIM610042 MeSHC567657 HERBHBDIS030060disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases
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Cryptogenic Partial Complex EpilepsyConditionTopicsyndrome MeSHD017029 HERBHBDIS011394disease · Nervous System Diseases
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Cryptogenic Tonic-Clonic EpilepsyConditionTopicsyndrome MeSHD004830 HERBHBDIS011162disease · Nervous System Diseases
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Dentatorubral-Pallidoluysian AtrophyConditionTopicsyndrome OMIM125370 MeSHD020191 HERBHBDIS011458disease · Nervous System Diseases
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Developmental Delay, Epilepsy, And Neonatal DiabetesConditionTopicsyndrome OMIM606176 MeSHC565253 HERBHBDIS016968disease · Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Behavior and Behavior Mechanisms; Endoc…
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Diabetes Mellitus, Permanent NeonatalConditionTopicsyndrome OMIM606176 MeSHC563425 HERBHBDIS015141disease · Nutritional and Metabolic Diseases; Endocrine System Diseases
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Digestive EpilepsyConditionTopicsyndrome MeSHD004828 HERBHBDIS028586disease · Nervous System Diseases
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Drug Resistant EpilepsyConditionTopicsyndrome MeSHD000069279 HERBHBDIS012582disease · Nervous System Diseases
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Early Childhood Epilepsy, MyoclonicConditionTopicsyndrome MeSHD004831 HERBHBDIS008700disease · Nervous System Diseases
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Early Infantile Epileptic Encephalopathy 6ConditionTopicsyndrome OMIM607208 HERBHBDIS027229disease · Nervous System Diseases
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Eating EpilepsyConditionTopicsyndrome HERBHBDIS028487disease · Nervous System Diseases
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Epilepsies, PartialConditionTopicsyndrome MeSHD004828 HERBHBDIS000957disease · Nervous System Diseases
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EpilepsyConditionTopicsyndrome ICD-10G40.9; G40 HPOHP:0001250 MeSHD004827 HERBHBDIS000956disease · Nervous System Diseases
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Epilepsy And MigraineConditionTopicsyndrome HERBHBDIS006505disease
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Epilepsy Co-Occurrent And Due To DementiaConditionTopicdisease HERBHBDIS028420disease · Mental Disorders; Nervous System Diseases
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Epilepsy In ChildrenConditionTopicsyndrome HERBHBDIS022514disease · Nervous System Diseases
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Epilepsy of Infancy With Migrating Focal SeizuresConditionTopicsyndrome HERBHBDIS026818disease · Nervous System Diseases
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Epilepsy With Grand Mal Seizures On Awakening (Disorder)ConditionTopicsyndrome HERBHBDIS028486disease · Nervous System Diseases
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Epilepsy With Myoclonic-Atonic SeizuresConditionTopicsyndrome HERBHBDIS027909disease
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Epilepsy, Absence, AtypicalConditionTopicsyndrome MeSHD004832 HERBHBDIS011168disease · Nervous System Diseases
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Epilepsy, AkineticConditionTopicsyndrome MeSHD004829 HERBHBDIS008421disease · Nervous System Diseases
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Epilepsy, Anterior Fronto-PolarConditionTopicsyndrome MeSHD017034 HERBHBDIS011396disease · Nervous System Diseases
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Epilepsy, AtonicConditionTopicsyndrome MeSHD004829 HERBHBDIS003391disease · Nervous System Diseases
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Epilepsy, Benign Neonatal, 1, And-Or MyokymiaConditionTopicsyndrome OMIM121200 MeSHC567743 HERBHBDIS019913disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
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Epilepsy, Benign Neonatal, 2ConditionTopicsyndrome OMIM121201 MeSHC535466 HERBHBDIS016891disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Epilepsy, Benign Neonatal, 3ConditionTopicsyndrome OMIM608217 MeSHC564274 HERBHBDIS015931disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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Epilepsy, Benign Psychomotor, ChildhoodConditionTopicsyndrome MeSHD004833 HERBHBDIS008693disease · Nervous System Diseases
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Epilepsy, Childhood Absence, 1ConditionTopicsyndrome OMIM600131 HERBHBDIS015696disease
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Epilepsy, Childhood Absence, Susceptibility To, 2ConditionTopicsyndrome OMIM607681 HERBHBDIS016009disease
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Epilepsy, Childhood Absence, Susceptibility To, 4ConditionTopicphenotype OMIM611136 MeSHC567002 HERBHBDIS018807phenotype · Nervous System Diseases