Epilepsy Ontology
2049 terms(s) returned
| Term Type: | Record: 851 to 900 of 2049 Records | Page: 18 of 41, First Previous Next Last | Show Records Per Page |
- cerebrospinal fluid sodium level
- cerebrovascular disease
- channel blocker-induced seizure
- chemical mutagenesis derived model
- childhood absence epilepsy
- childhood epilepsy with occipital paroxysm
- childhood-onset epilepsy syndrome
- chromosomal anomaly
- chromosome 15q13.3 microdeletion syndrome
- chromosome 18q deletion syndrome
- chromosome 1p36 deletion syndrome
- chronic pain
- chronic spontaneous limbic seizure model
- cingulate cortex
- cingulate cortex seizure
- cingulate epilepsy
- cingulate sulcus
- circadian rhythm sleep disorder
- claudication
- clinical data item
- clinical finding
- clinical history
- clinical measurement
- closeMatch
- coagulopathy AE
- cobalt model
- code
- cognitive aura
- cognitive behavior
- cognitive disorder
- cognitive process
- cognitive symptom
- combined generalized and focal epilepsy
- comment
- commissure of telencephalon
- communication disorder
- comorbidity
- complex febrile model
- complex visual hallucination
- composite part spanning multiple base regional parts of brain
- compulsive valsalva
- confusion
- congenital abnormality
- congenital heart disease
- congenital nervous system abnormality
- congenital stroke
- congestive heart failure
- connective tissue disease
- connectivity
- consciousness behavior
