Alkylglycerone-phosphate synthase deficiency

MONDO:0100274

Any disorder of plasmalogen biosynthesis in which the cause of the disease is a mutation in the AGPS gene.

Also known as: AGPS deficiency, alkylglycerone-phosphate synthase deficiency

2 clinical trials for this condition and its sub-types, 0 tagged with Alkylglycerone-phosphate synthase deficiency itself.

Where it sits in the disease tree

Part of

Sub-types of Alkylglycerone-phosphate synthase deficiency

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