DISEASES

Disease-gene associations mined from literature

Human genes for glycine encephalopathy

Glycine encephalopathy [DOID:9268]

An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues.

Synonyms:  glycine encephalopathy,  DOID:9268,  glycine encephalopathies,  nonketotic hyperglycinemia,  Non-ketotic hyperglycinemia ...

Linkouts:  OMIM