About   Help   FAQ
Disease Ontology Browser
ornithine carbamoyltransferase deficiency (DOID:9271)
Alliance: disease page
Synonyms: deficiency of citrulline phosphorylase; ornithine transcarbamylase deficiency
Alt IDs: OMIM:311250, ICD10CM:E72.4, MESH:D020163, NCI:C84957, UMLS_CUI:C0268542
Definition: An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase.

Disease References using Mouse Models (10)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory