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[X] hereditary lethal multiple congenital anomalies/dysmorphic syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0043009

An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: genetic lethal multiple congenital anomalies/dysmorphic syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:471383 (MONDO:equivalentTo)
  • UMLS:C5681265 (MONDO:equivalentTo)
  • MEDGEN:1843298 (MONDO:equivalentTo)
  • GARD:21947 (MONDO:GARD)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, disease_grouping, 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

exactMatch

http://www.orpha.net/ORDO/Orphanet_471383

http://identifiers.org/medgen/1843298

http://linkedlifedata.com/resource/umls/id/C5681265

id

MONDO:0043009

Term relations