glycine encephalopathy Disease Ontology Browser

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Disease Ontology Browser

glycine encephalopathy (DOID:9268)
Alliance: disease page
Synonyms: Non-ketotic hyperglycinemia; nonketotic hyperglycinemia
Alt IDs: OMIM:605899, ICD10CM:E72.51, MESH:D020158, NCI:C84937, UMLS_CUI:C0751748
Definition: An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues.

Disease References using Mouse Models (2)

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

Allelic Composition	Genetic Background	Reference	Phenotypes
GldcGt(EUCG0001d02)Hmgu/GldcGt(EUCG0001d02)Hmgu	B6.129P2-Gldc^{Gt(EUCG0001d02)Hmgu}	J:221782	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Slc6a9tm1Betz/Slc6a9tm1Betz	involves: 129P2/OlaHsd * C57BL/6	J:86624	View