An inherited disorder that affects the metabolism of any acidic compound containing carbon in a covalent linkage. [ NCIT:C101334 ]
Synonyms: inborn organic acid metabolic process disorder inborn error of organic acid metabolic process organic acidemia rare inborn error of organic acid metabolic process organic aciduria
Term information
- MEDGEN:66037 (MONDO:equivalentTo)
- UMLS:C0241775 (MONDO:equivalentTo)
- NCIT:C101334 (MONDO:equivalentTo)
- icd11.foundation:1921636230 (https://orcid.org/0000-0002-4142-7153)
- ICD9:277.89 (MONDO:relatedTo)
- GARD:9433 (MONDO:GARD)
- Orphanet:289899 (MONDO:equivalentTo)
- DOID:0060159 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://identifiers.org/medgen/66037
http://purl.obolibrary.org/obo/DOID_0060159
http://linkedlifedata.com/resource/umls/id/C0241775
http://www.orpha.net/ORDO/Orphanet_289899
http://purl.obolibrary.org/obo/NCIT_C101334