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Noonan syndrome and Noonan-related syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0020297

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1826127 (MONDO:equivalentTo)
  • Orphanet:98733 (MONDO:equivalentTo)
  • GARD:19561 (MONDO:GARD)
  • UMLS:C5681679 (MONDO:equivalentTo)
  • MESH:C537846 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_included, matrix_txgnn_grouping_member, rare, mondo_top_grouping_cardiovascular_disorder, harrisons_view_musculoskeletal_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cardiovascular_disorder, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C5681679

http://identifiers.org/mesh/C537846

http://identifiers.org/medgen/1826127

http://www.orpha.net/ORDO/Orphanet_98733

id

MONDO:0020297