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[X] developmental defect during embryogenesis

Go to external page http://purl.obolibrary.org/obo/MONDO_0019755

A disease that has its basis in the disruption of embryonic morphogenesis. [ MONDO:design_pattern ]

Synonyms: embryonic morphogenesis disease rare developmental defect during embryogenesis congenital malformation syndrome malformation syndrome developmental defect during embryogenesis disorder of embryonic morphogenesis

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1825997 (MONDO:equivalentTo)
  • SCTID:400038003 (MONDO:equivalentTo)
  • UMLS:C5680284 (MONDO:equivalentTo)
  • Orphanet:93890 (MONDO:equivalentTo)
  • NCIT:C99267 (MONDO:equivalentTo)
  • ICD9:759.7
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, disease_grouping, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/NCIT_C99267

http://www.orpha.net/ORDO/Orphanet_93890

http://linkedlifedata.com/resource/umls/id/C5680284

http://identifiers.org/medgen/1825997

http://identifiers.org/snomedct/400038003

id

MONDO:0019755