Answer | None | LA137-2 |
Answer | CIT-I or CIT-II or ASA | LA12569-2 |
Answer | HCY or MET or CBL C | LA12570-0 |
Answer | PKU or BIPT-BS or BIOPT-REG or H-PHE | LA12571-8 |
Answer | TYR-1 or TYR-II or TYR-III | LA12572-6 |
Answer | Maple syrup urine disease | LA21168-2 |
Answer | Argininemia | LA21161-7 |
Answer | Argininosuccinic aciduria | LA21162-5 |
Answer | Carbamoyl-phosphate synthase deficiency | LA12484-4 |
Answer | Citrullinemia, type I | LA12482-8 |
Answer | Citrullinemia, type II | LA12483-6 |
Answer | Dihydrolipoamide dehydrogenase deficiency | LA12490-1 |
Answer | Biopterin defect in cofactor biosynthesis | LA12472-9 |
Answer | Biopterin defect in cofactor regeneration | LA12473-7 |
Answer | Girate atrophy of the retina | LA12502-3 |
Answer | Hypermethioninemia | LA12512-2 |
Answer | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | LA12497-6 |
Answer | Hyperphenylalaninemia (variant, benign) | LA12500-7 |
Answer | Hyperprolinemia type I | LA12521-3 |
Answer | Hyperprolinemia type II | LA12522-1 |
Answer | Cobalamin E disease | LA12480-2 |
Answer | Guanidinoacetate N-methyltransferase deficiency | LA30113-7 |
Answer | L-arginine:glycine amidinotransferase deficiency | LA30114-5 |
Answer | Methylene tetrahydrofolate reductase deficiency | LA12514-8 |
Answer | Nonketotic hyperglycinemia (glycine encephalopathy) | LA12516-3 |
Answer | Ornithine transcarbamylase deficiency | LA12518-9 |
Answer | Classic phenylketonuria | LA12520-5 |
Answer | Pyroglutamic acidemia | LA12469-5 |
Answer | Pyruvate carboxylase deficiency | LA12519-7 |
Answer | Tyrosinemia, type I | LA12528-8 |
Answer | Tyrosinemia, type II | LA12529-6 |
Answer | Tyrosinemia, type III | LA12530-4 |
Answer | Valinemia | LA12503-1 |
Answer | X-linked creatine transporter (CRTR) deficiency | LA30492-5 |
answers-for | Amino acidemia disorder suspected [Identifier] in DBS | 57793-2 |
LONG_COMMON_NAME | en-US | NBS AA susc |
LOINC Version: 2.77