An inherited metabolic disease that is has its basis in the disruption of serine family amino acid metabolic process.
Comprehensive, easy-to-understand information about this condition
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inborn disorder of amino acid metabolism
MONDO:0004736
glycine encephalopathy
MONDO:0011612
pyruvate metabolism disorder
MONDO:0016789
inborn disorder of lysine and hydroxylysine metabolism
MONDO:0017351
disorder of glutamine metabolism
MONDO:0017352
disorder of beta and omega amino acid metabolism
MONDO:0017684