Also Known As:
Rhizomelic chondrodysplasia punctata, type 2; Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency; Chondrodysplasia punctata, rhizomelic, due to DHAPAT deficiency; DHAPAT deficiency; Dihydroxyacetonephosphate acyltransferase deficiency; GNPAT deficiency; Glyceronephosphate O-Acyltransferase Deficiency; Glyceronephosphate acyltransferase deficiency; Human dihydroxyacetonephosphate acyltransferase deficiency; Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency; Type 2 rhizomelic chondrodysplasia punctata