Epilepsy Ontology
280 terms(s) returned
Term Type: Class | Record: 51 to 100 of 280 Records | Page: 2 of 6, First Previous Next Last | Show Records Per Page |
- autosomal dominant disease
- autosomal dominant nocturnal frontal lobe epilepsy
- autosomal genetic disease
- bacterial infectious disease
- benign epilepsy with centrotemporal spikes
- benign familial infantile epilepsy
- benign neoplasm
- bipolar disorder
- bladder disease
- bone disease
- bone inflammation disease
- brain angioma
- brain cancer
- brain disease
- brain edema
- brain glioma
- brain infarction
- brain ischemia
- bronchial disease
- bruxism
- bullous pemphigoid
- carbohydrate metabolic disorder
- carbohydrate metabolism disease
- cardiac arrest
- cardiomyopathy
- cardiovascular organ benign neoplasm
- cardiovascular system disease
- celiac disease
- cell type benign neoplasm
- cellulitis
- central nervous system benign neoplasm
- central nervous system cancer
- central nervous system disease
- cerebral angioma
- cerebral infarction
- cerebral malaria
- cerebral palsy
- cerebrovascular disease
- childhood absence epilepsy
- chromosome 15q13.3 microdeletion syndrome
- chromosome 18q deletion syndrome
- chromosome 1p36 deletion syndrome
- cognitive disorder
- communication disorder
- congenital heart disease
- congenital nervous system abnormality
- congestive heart failure
- connective tissue disease
- conversion disorder
- coronary artery disease