JSON

[X] lipodystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0006573

A congenital or acquired disorder characterized by abnormal loss or redistribution of the adipose tissue in the body. [ NCIT:P378 ]

Synonyms: lipodsystrophic syndrome lipodystrophy (disease) lipodystrophy lipodsystrophic syndromes

This is just here as a test because I lose it

Term information

database cross reference
  • NANDO:1200858 (https://orcid.org/0000-0003-0011-764X)
  • MESH:D008060 (MONDO:equivalentTo)
  • UMLS:C0023787 (MONDO:equivalentTo)
  • EFO:1000727 (MONDO:equivalentTo)
  • DOID:811 (MONDO:equivalentTo)
  • MEDGEN:6111 (MONDO:equivalentTo)
  • HP:0009125 (MONDO:otherHierarchy)
  • NCIT:C97093 (MONDO:equivalentTo)
  • NANDO:2200404 (https://orcid.org/0000-0003-0011-764X)
  • ICD9:272.6 (MONDO:i2s)
  • SCTID:71325002 (MONDO:equivalentTo)
  • Wikipedia:Lipodystrophy (EFO:1000727)
  • NANDO:2100147 (https://orcid.org/0000-0003-0011-764X)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, 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, harrisons_view_member, harrisons_view_integumentary_system_disorder, harrisons_view_metabolic_disease

OBO foundry unique label

lipodystrophy (disease)

exactMatch

http://www.ebi.ac.uk/efo/EFO_1000727

http://purl.obolibrary.org/obo/NCIT_C97093

http://identifiers.org/snomedct/71325002

http://identifiers.org/medgen/6111

http://linkedlifedata.com/resource/umls/id/C0023787

http://identifiers.org/mesh/D008060

http://purl.obolibrary.org/obo/DOID_811

id

MONDO:0006573