General Information of Disease (ID: DIS5BDC1)

Disease Name Inborn disorder of ornithine metabolism
Synonyms inborn error of ornithine metabolic process; rare inborn error of ornithine metabolic process; disorder of ornithine metabolism; inborn ornithine metabolic process disorder
Definition An inherited metabolic disease that is has its basis in the disruption of ornithine metabolic process.
Disease Hierarchy
DISFWXCM: Inborn disorder of amino acid metabolism
DISO5FAY: Inborn error of metabolism
DISDTQA4: Inborn disorder of ornithine or proline metabolism
DISTVTFI: Disorder of organic acid metabolism
DIS5BDC1: Inborn disorder of ornithine metabolism
Disease Identifiers
MONDO ID
MONDO_0017356
UMLS CUI
C0342690
MedGen ID
575181
Orphanet ID
289869
SNOMED CT ID
237928008