Any disorder of plasmalogen biosynthesis in which the cause of the disease is a mutation in the GNPAT gene.
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rhizomelic chondrodysplasia punctata type 2
MONDO:0009112
rhizomelic chondrodysplasia punctata
MONDO:0015776
acyl-CoA binding domain containing protein 5 deficiency
MONDO:0100112
alkylglycerone-phosphate synthase deficiency
MONDO:0100274
fatty acyl-CoA reductase defects
MONDO:0100275