JSON

[X] multiple congenital anomalies/dysmorphic syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0019042

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5681310 (MONDO:equivalentTo)
  • MEDGEN:1843247 (MONDO:equivalentTo)
  • GARD:18876 (MONDO:GARD)
  • Orphanet:68341 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__txgnn_other, mondo_top_grouping_member, 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, rare, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, ordo_group_of_disorders

abbreviation
MCAHS [ MONDO:Lexical ]

exactMatch

http://identifiers.org/medgen/1843247

http://linkedlifedata.com/resource/umls/id/C5681310

http://www.orpha.net/ORDO/Orphanet_68341

id

MONDO:0019042

term tracker item

https://github.com/monarch-initiative/mondo/issues/4069