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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
urea cycle disorder +     
3-methylcrotonyl-CoA carboxylase deficiency +   
argininosuccinic aciduria  
autosomal recessive osteopetrosis 3  
carbamoyl phosphate synthetase I deficiency disease  
Citrulline Transport Defect 
citrullinemia +   
hyperargininemia  
An urea cycle disorder that involves arginase deficiency resulting in elevated levels of plasma arginine. (DO)
N-acetylglutamate synthase deficiency  
ornithine carbamoyltransferase deficiency  
ornithine translocase deficiency  

Synonyms
Exact Synonyms: ARG1 Deficiency ;   ARG1 deficiencies ;   Arginase Deficiency ;   Arginase Deficiency Disease ;   arginase deficiencies ;   arginase deficiency diseases ;   argininemia ;   deficiency of canavanase ;   hyperargininemias
Primary IDs: MESH:D020162
Alternate IDs: OMIM:207800
Xrefs: ICD10CM:E72.21 ;   NCI:C84568
Definition Sources: https://www.medlink.com/articles/hyperargininemia "DO" "DO"

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