JSON

meningoencephalocele

Go to external page http://purl.obolibrary.org/obo/MONDO_0017079

A congenital abnormality in which the meninges protrude through a defect in the cranium. [ NCIT:C124517 ]

Synonyms: meningoencephalocele cephalocele (disease) of brain meninx brain meninx cephalocele (disease)

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:Q01.2 (Orphanet:268820/ntbt)
  • ICD10CM:Q01.0 (Orphanet:268820/ntbt)
  • GARD:20968 (MONDO:GARD)
  • SCTID:52330001 (MONDO:equivalentTo)
  • NANDO:2200813 (https://orcid.org/0000-0003-0011-764X)
  • UMLS:C0266456 (MONDO:equivalentTo)
  • MEDGEN:82743 (MONDO:equivalentTo)
  • NCIT:C124517 (MONDO:equivalentTo)
  • Orphanet:268820 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, ordo_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, ordo_morphological_anomaly, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_included, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis, orphanet_rare, harrisons_view_nervous_system_disorder

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/location.yaml

exactMatch

http://linkedlifedata.com/resource/umls/id/C0266456

http://identifiers.org/medgen/82743

http://www.orpha.net/ORDO/Orphanet_268820

http://purl.obolibrary.org/obo/NCIT_C124517

http://identifiers.org/snomedct/52330001

excluded from qc check

http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql

has related synonym

cranial meningocele

encephalomeningocele

id

MONDO:0017079