Inborn disorder of serine family metabolism

rare

An inherited metabolic disease that is has its basis in the disruption of serine family amino acid metabolic process.

Identifiers: MONDO:0019239 Orphanet:79194
Part of: Inborn disorder of amino acid and other organic acid metabolism
Also known as: inborn disorder of serine or glycine metabolism · inborn error of serine family amino acid metabolic process · inborn serine family amino acid metabolic process disorder · rare inborn error of serine family amino acid metabolic process

Subtypes

Disease	ID	Subtypes
Neurometabolic disorder due to serine deficiency	MONDO:0018162	10
Glycine encephalopathy	MONDO:0011612	6
Inborn disorder of glycine and serine metabolism	MONDO:0800155

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