Also known as Non-ketotic hyperglycinemia, Non-ketotic hyperglycinemia (disorder), nonketotic hyperglycinemia, Glycine synthase deficiency, Hyperglycinemia, Transient Neonatal, GLYCINE ENCEPHALOPATHY; GCE, GCE
amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues
via PubMed
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).