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[X] inborn disorder of tryptophan metabolism

Go to external page http://purl.obolibrary.org/obo/MONDO_0017350

An inherited metabolic disease that is has its basis in the disruption of tryptophan metabolic process. [ MONDO:patterns/inborn_metabolic ]

Synonyms: inborn error of tryptophan metabolic process rare inborn error of tryptophan metabolic process inborn tryptophan metabolic process disorder

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:22506 (MONDO:equivalentTo)
  • GARD:21154 (MONDO:GARD)
  • SCTID:5181007 (MONDO:equivalentTo)
  • ICD9:270.2 (MONDO:relatedTo)
  • icd11.foundation:282654317 (https://orcid.org/0000-0002-4142-7153)
  • UMLS:C0041254 (MONDO:equivalentTo)
  • Orphanet:289829 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_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, ordo_group_of_disorders, harrisons_view_metabolic_disease

conformsTo

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

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

exactMatch

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/282654317

http://www.orpha.net/ORDO/Orphanet_289829

http://identifiers.org/medgen/22506

http://linkedlifedata.com/resource/umls/id/C0041254

http://identifiers.org/snomedct/5181007

has related synonym

disorder of tryptophan metabolism

id

MONDO:0017350