Glycine encephalopathy

MONDO:0011612

Glycine encephalopathy (GE) is an inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and tissues, including the brain, resulting in neurometabolic symptoms of variable severity.

Also known as: NKA, Nonketotic Hyperglycinemia, glycine encephalopathy, non-ketotic hyperglycinemia, nonketotic hyperglycinemia, GCE, GLYCINE encephalopathy, Glycine synthase deficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Glycine encephalopathy itself.

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↑ Brain disorder (16709) ↑ Hereditary neurological disease (5791) ↑ Inborn disorder of amino acid metabolism (159) ↑ Inborn disorder of serine family metabolism (1)

Sub-types of Glycine encephalopathy

Atypical glycine encephalopathy 0 trials
Glycine encephalopathy 1 0 trials
Glycine encephalopathy 2 0 trials
Infantile glycine encephalopathy 0 trials
Neonatal glycine encephalopathy 0 trials

Including sub-types (0) Tagged with Glycine encephalopathy (0)

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