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complex neurodevelopmental disorder

Go to external page http://purl.obolibrary.org/obo/MONDO_0100038

A disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy). [ https://orcid.org/0000-0002-6733-369X https://www.clinicalgenome.org/working-groups/clinical-domain/neurodevelopmental-disorders/ ]

Synonyms: complex neurodevelopmental disorder

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1800189 (MONDO:equivalentTo)
  • GARD:17965 (MONDO:GARD)
  • Orphanet:528084 (MONDO:equivalentTo)
  • UMLS:C5568766 (MONDO:equivalentTo)
Subsets

ordo_disorder, matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, matrix_llm__tag_existing_treatment_other, matrix_included, 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, orphanet_rare, harrisons_view_nervous_system_disorder

ClinGen label
complex neurodevelopmental disorder [ Orphanet:528084 ]

creator

https://orcid.org/0000-0001-5208-3432

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0100038

date

2018-06-29T18:21:11Z

exactMatch

http://linkedlifedata.com/resource/umls/id/C5568766

http://www.orpha.net/ORDO/Orphanet_528084

http://identifiers.org/medgen/1800189

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019117

id

MONDO:0100038

term tracker item

https://github.com/monarch-initiative/mondo/issues/7308

https://github.com/monarch-initiative/mondo/issues/3680

Term relations