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[X] familial partial epilepsy

Go to external page http://purl.obolibrary.org/obo/MONDO_0017704

An instance of partial epilepsy that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: hereditary partial epilepsy

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:309 (MONDO:equivalentTo)
  • GARD:2173 (MONDO:GARD)
  • MEDGEN:1826100 (MONDO:equivalentTo)
  • UMLS:C5680862 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, harrisons_view_nervous_system_disorder, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C5680862

http://identifiers.org/medgen/1826100

http://www.orpha.net/ORDO/Orphanet_309

has related synonym

epilepsy, partial, familial

id

MONDO:0017704

seeAlso

https://rarediseases.info.nih.gov/diseases/2173/epilepsy-partial-familial