JSON

[X] hereditary lipodystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0020087

An instance of lipodystrophy that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]

Synonyms: genetic lipodystrophy (disease) genetic lipodystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • icd11.foundation:1166232738 (https://orcid.org/0000-0002-3458-4839)
  • SCTID:724841000 (MONDO:equivalentTo)
  • Orphanet:98305 (MONDO:equivalentTo)
  • UMLS:C4511302 (MONDO:equivalentTo)
  • GARD:12597 (MONDO:GARD)
  • MEDGEN:1383706 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, disease_grouping, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease, harrisons_view_integumentary_system_disorder, ordo_group_of_disorders, harrisons_view_metabolic_disease

conformsTo

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

exactMatch

http://identifiers.org/medgen/1383706

http://identifiers.org/snomedct/724841000

http://linkedlifedata.com/resource/umls/id/C4511302

http://www.orpha.net/ORDO/Orphanet_98305

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1166232738

id

MONDO:0020087