Answer | None | LA137-2 |
Answer | Carnitine palmitoyltransferase type I deficiency | LA12485-1 |
Answer | Carnitine uptake deficiency/carnitine transport defect | LA12487-7 |
Answer | CPT-II or CACT | LA12573-4 |
Answer | LCHAD or TFP | LA12574-2 |
Answer | Medium-chain acyl-CoA dehydrogenase deficiency | LA12509-8 |
Answer | MCAD or SCAD or GA-2(MADD) | LA12575-9 |
Answer | SCAD or EMA or IBG or GA-2 (MADD) | LA12576-7 |
Answer | Very long-chain acyl-CoA dehydrogenase deficiency | LA12531-2 |
Answer | 2,4-Dienoyl-CoA reductase deficiency | LA12489-3 |
Answer | Carnitine acylcarnitine translocase deficiency | LA12475-2 |
Answer | Carnitine palmitoyltransferase type II deficiency | LA12486-9 |
Answer | Glutaric acidemia type II | LA12495-0 |
Answer | Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency | LA12507-2 |
Answer | Carnitine uptake deficiency/carnitine transport defect (maternal) | LA12488-5 |
Answer | Medium-chain ketoacyl-CoA thiolase deficiency | LA12511-4 |
Answer | Short-chain acyl-CoA dehydrogenase deficiency | LA12524-7 |
Answer | Short-chain L-3-hydroxy acyl-CoA dehydrogenase deficiency | LA12525-4 |
Answer | Trifunctional protein deficiency | LA12527-0 |
Answer | CUD or CUD (mat) or CPT-Ia | LA12916-5 |
Answer | GA-1 or GA-2 | LA12917-3 |
Answer | X-linked adrenoleukodystrophy | LA25796-6 |
answers-for | Fatty acid oxidation conditions suspected [Identifier] in DBS | 57792-4 |
LONG_COMMON_NAME | en-US | NBS FA susc |
LOINC Version: 2.77