[X] inborn disorder of amino acid transport
Go to external page http://purl.obolibrary.org/obo/MONDO_0019216
Synonyms: inborn disorder of amino acid absorption and transport
Term information
- icd11.foundation:1631611896 (https://orcid.org/0000-0001-5208-3432)
- UMLS:C0268641 (MONDO:equivalentTo)
- ICD9:270.0 (MONDO:i2s)
- GARD:18948 (MONDO:GARD)
- Orphanet:79166 (MONDO:equivalentTo)
- SCTID:16784003 (MONDO:equivalentTo)
- MEDGEN:541381 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_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
http://identifiers.org/snomedct/16784003
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1631611896
http://www.orpha.net/ORDO/Orphanet_79166
http://linkedlifedata.com/resource/umls/id/C0268641
http://identifiers.org/medgen/541381