inborn disorder of methionine cycle and sulfur amino acid metabolism
Go to external page http://purl.obolibrary.org/obo/MONDO_0019222
An inherited metabolic disease that is has its basis in the disruption of sulfur amino acid metabolic process. [ MONDO:patterns/inborn_metabolic ]
Synonyms: inborn sulfur amino acid metabolic process disorder inborn sulphur amino acid metabolic process disorder inborn error of sulfur amino acid metabolic process cytosolic methyl group transfer or sulfur amino acid metabolism disorder rare inborn error of sulfur amino acid metabolic process inborn error of sulphur amino acid metabolic process rare inborn error of sulphur amino acid metabolic process cytosolic methyl group transfer or sulphur amino acid metabolism disorder
Term information
- UMLS:CN227589 (MONDO:equivalentTo)
- Orphanet:79173 (MONDO:equivalentTo)
- SCTID:28882002 (MONDO:equivalentTo)
- ICD9:270.4 (MONDO:i2s)
- GARD:18953 (Orphanet:79173)
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders
http://identifiers.org/snomedct/28882002
http://www.orpha.net/ORDO/Orphanet_79173
http://linkedlifedata.com/resource/umls/id/CN227589
disorder of methionine cycle and sulphur amino acid metabolism
disorder of methionine cycle and sulfur amino acid metabolism