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[X] non-syndromic amelia

Go to external page http://purl.obolibrary.org/obo/MONDO_0017419

A congenital malformation characterized by the complete absence of all limbs. [ NCIT:C34370 ]

Synonyms: nonsyndromic amelia

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:21179 (MONDO:GARD)
  • NCIT:C34370 (MONDO:equivalentTo)
  • Orphanet:294925 (MONDO:equivalentTo)
  • UMLS:C0002447 (MONDO:equivalentTo)
  • MEDGEN:8014 (MONDO:equivalentTo)
  • HP:0009827 (MONDO:otherHierarchy)
  • SCTID:62588002 (MONDO:equivalentTo)
  • MedDRA:10001926 (Orphanet:294925/e)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_musculoskeletal_system_disorder, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10001926

exactMatch

http://identifiers.org/medgen/8014

http://purl.obolibrary.org/obo/NCIT_C34370

http://linkedlifedata.com/resource/umls/id/C0002447

http://www.orpha.net/ORDO/Orphanet_294925

http://identifiers.org/snomedct/62588002

has related synonym

isolated amelia

id

MONDO:0017419

term tracker item

https://github.com/monarch-initiative/mondo/issues/6751