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childhood-onset epilepsy syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0020072

A epilepsy syndrome that occurs during childhood. [ MONDO:design_pattern ]

Synonyms: paediatric epilepsy syndrome childhood epilepsy syndrome epilepsy syndrome of childhood childhood-onset epilepsy syndrome pediatric epilepsy syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1843031 (MONDO:equivalentTo)
  • UMLS:C5681526 (MONDO:equivalentTo)
  • GARD:19437 (MONDO:GARD)
  • Orphanet:98259 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, matrix_included, nord_rare, matrix_llm__tag_existing_treatment_other, clingen, 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_nervous_system_disorder, ordo_group_of_disorders

UK spelling synonym
paediatric epilepsy syndrome

ClinGen label
childhood-onset epilepsy syndrome [ Orphanet:98259 ]

comment

This type of grouping class represents an older way of classifying diseases, and represented here https://www.epilepsydiagnosis.org/index.html.

contributor

https://orcid.org/0000-0002-4142-7153

https://orcid.org/0000-0003-2955-4640

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0020072

exactMatch

http://linkedlifedata.com/resource/umls/id/C5681526

http://www.orpha.net/ORDO/Orphanet_98259

http://identifiers.org/medgen/1843031

id

MONDO:0020072

term tracker item

https://github.com/monarch-initiative/mondo/issues/1640