About   Help   FAQ
Disease Ontology Browser
combined oxidative phosphorylation deficiency 19 (DOID:0111476)
Alliance: disease page
Synonyms: COXPD19; severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
Alt IDs: OMIM:615595, ORDO:397593
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the LYRM4 gene on chromosome 6p25.1.

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
MGI 6.24
The Jackson Laboratory