FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term ornithine carbamoyltransferase deficiency ID (Ontology) DOID:9271 (Human Disease)
Definition An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase.
Also Known As "deficiency of citrulline phosphorylase" ; "ornithine transcarbamylase deficiency"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
  amino acid metabolic disorder
   |__urea cycle disorder
       |__ornithine carbamoyltransferase deficiency
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a urea cycle disorder
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "deficiency of citrulline phosphorylase" EXACT
    "ornithine transcarbamylase deficiency" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:8391
ICD10CM:E72.4
MESH:D020163
MIM:311250
NCI:C84957
SNOMEDCT_US_2023_03_01:80908008
UMLS_CUI:C0268542