JSON

lymphatic malformation

Go to external page http://purl.obolibrary.org/obo/MONDO_0019313

Primary lymphedema is caused by anatomic or functional defects in the lymphatic system, resulting in chronic swelling of body parts and lymphatic-system malformation. [ http://www.ncbi.nlm.nih.gov/pubmed/22831870 ]

Synonyms: hereditary lymphedema lymphedema, hereditary

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:757.0 (DOID:0050580)
  • MEDGEN:140763 (MONDO:equivalentTo)
  • DOID:0050580 (MONDO:equivalentTo)
  • UMLS:C0398368 (MONDO:equivalentTo)
  • SCTID:254199006 (MONDO:equivalentTo)
  • OMIMPS:153100 (https://orcid.org/0000-0002-6601-2165)
  • GARD:13057 (MONDO:GARD)
  • ICD10CM:Q82.0 (Orphanet:79452/ntbt)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, harrisons_view_immune_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, icd10_billable, matrix_txgnn_grouping_member, harrisons_view_cardiovascular_disorder, rare, mondo_top_grouping_immune_system_disorder, mondo_top_grouping_cardiovascular_disorder, harrisons_view_member, harrisons_view_hereditary_disease

exactMatch

http://identifiers.org/snomedct/254199006

http://linkedlifedata.com/resource/umls/id/C0398368

http://purl.bioontology.org/ontology/ICD10CM/Q82.0

https://omim.org/phenotypicSeries/PS153100

http://identifiers.org/medgen/140763

http://purl.obolibrary.org/obo/DOID_0050580

id

MONDO:0019313

should conform to

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

term tracker item

https://github.com/monarch-initiative/mondo/issues/6877

https://github.com/monarch-initiative/mondo/issues/6740