Term info
database cross reference
- UMLS:CN227601 (MONDO:equivalentTo)
- Orphanet:79194 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An inherited metabolic disease that is has its basis in the disruption of serine family amino acid metabolic process.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_79194, http://linkedlifedata.com/resource/umls/id/CN227601
has exact synonym
inborn serine family amino acid metabolic process disorder, inborn error of serine family amino acid metabolic process, inborn disorder of serine or glycine metabolism, rare inborn error of serine family amino acid metabolic process
has related synonym
disorder of serine or glycine metabolism
id
MONDO:0019239