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Diagnosis
3-Methylcrotonyl CoA Carboxylase Deficiency (3MCC)
Arginase Deficiency (ARG)
Argininosuccinic Acidemia (ASA)
Citrullinaemia
Glutaric Acidaemia Type 1 (GA1)
Homocystinuria (HCU)
Isovaleric Aciduria (IVA)
Maple Syrup Urine Disease (MSUD)
Methylmalonic Aciduria (MMA)
Ornithine Transcarbamylase Deficiency (OTC)
Phenylketonuria (PKU)
Propionic Acidaemia (PA)
Tyrosinaemia Type 1 & 2 (TYRO)
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