About   Help   FAQ
Disease Ontology Browser
holocarboxylase synthetase deficiency (DOID:859)
Alliance: disease page
Synonyms: Biotin-(propionyl-CoA-carboxylase) ligase deficiency; Multiple carboxylase deficiency - neonatal onset
Alt IDs: OMIM:253270, ICD10CM:D81.818, MESH:D028922, NCI:C98842, UMLS_CUI:C0268581
Definition: A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase.


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
03/19/2024
MGI 6.23
The Jackson Laboratory