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inborn disorder of serine family metabolism

Go to external page http://purl.obolibrary.org/obo/MONDO_0019239

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

Synonyms: 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

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:18968 (Orphanet:79194)
  • UMLS:CN227601 (MONDO:equivalentTo)
  • Orphanet:79194 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/CN227601

http://www.orpha.net/ORDO/Orphanet_79194

has related synonym

disorder of serine or glycine metabolism

id

MONDO:0019239