Para efectos de este capítulo, errores innatos del metabolismo significa trastornos hereditarios que padece una persona desde su nacimiento, los cuales incluye que padezcan del trastorno genético denominado como fenilcetonuria (PKU, por sus siglas en inglés), las diferentes aminoacidopatías, las acidemias orgánicas, los desórdenes de oxidación de ácidos grasos, los desórdenes del metabolismo de carbohidratos (como la galactosemia) y las deficiencias de cofactores enzimáticos (como la deficiencia de biotinidasa) incluidas en el Programa de Cernimiento Metabólico Neonatal autorizado por las secs. 3151 et seq. de este título.
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