A non-syndromic amelia that involves the hindlimb. [ MONDO:patterns/location ]

Synonyms: hindlimb non-syndromic amelia non-syndromic amelia of hindlimb

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:539370 (MONDO:equivalentTo)
  • SCTID:265798000 (MONDO:equivalentTo)
  • Orphanet:294969 (MONDO:equivalentTo)
  • UMLS:C0265621 (MONDO:equivalentTo)
  • icd11.foundation:540310468 (Orphanet:294969)
  • HP:0009818 (MONDO:otherHierarchy)
  • GARD:21191 (MONDO:GARD)
Subsets

gard_rare, ordo_disorder, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, ordo_morphological_anomaly, matrix_included, 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, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis, orphanet_rare

conformsTo

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

exactMatch

http://linkedlifedata.com/resource/umls/id/C0265621

http://identifiers.org/snomedct/265798000

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/540310468

http://identifiers.org/medgen/539370

http://www.orpha.net/ORDO/Orphanet_294969

id

MONDO:0017438