An inherited disorder in which the body cannot process a particular protein building block (amino acid) called Methionine. It can be caused by several different genes.
Hypermethioninemia (MET)
An inherited disorder in which the body cannot process a particular protein building block (amino acid) called Methionine.
Phenylketonuria (PKU) and HyperPHE
An inherited disorder in which the body cannot process a particular protein building block (amino acid) called Phenylalanine.
Pyruvate Carboxylase deficiency
An inherited disorder in which the body cannot process a protein building block called amino acids and makes very high lactic acid because of the enzyme deficiency.
Tyrosinemia I (TYR 1)
An inherited disorder in which the body cannot process a particular protein building block (amino acid) called Tyrosine. This disorder leads to liver toxins building up that can lead to death if not treated early. There is also Type II and III that are milder.
