Synonyms: TRPS

This is just here as a test because I lose it

Term information

database cross reference
  • OMIMPS:190350 (MONDO:equivalentTo)
  • UMLS:C0265255 (MONDO:equivalentTo)
  • Orphanet:324764 (MONDO:equivalentTo)
  • SCTID:18077009 (MONDO:equivalentTo)
  • ICD9:759.89 (MONDO:relatedTo)
  • GARD:21451 (MONDO:GARD)
  • MEDGEN:539179 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, disease_grouping, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, rare, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_syndromic_disease, harrisons_view_integumentary_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, ordo_group_of_disorders

abbreviation
TRPS [ MONDO:Lexical ]

exactMatch

https://omim.org/phenotypicSeries/PS190350

http://linkedlifedata.com/resource/umls/id/C0265255

http://identifiers.org/medgen/539179

http://www.orpha.net/ORDO/Orphanet_324764

http://identifiers.org/snomedct/18077009

id

MONDO:0017951

should conform to

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