Term info
database cross reference
- UMLS:CN227178 (MONDO:equivalentTo)
- GARD:0002173 (MONDO:equivalentTo)
- Orphanet:309 (MONDO:equivalentTo)
Subsets
gard_rare, disease_grouping, ordo_group_of_disorders
definition
An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_309, http://linkedlifedata.com/resource/umls/id/CN227178
has exact synonym
hereditary partial epilepsy
has related synonym
epilepsy, partial, familial
id
MONDO:0017704
seeAlso
https://rarediseases.info.nih.gov/diseases/2173/epilepsy-partial-familial