What is another word for Hydroxyphenylpyruvate Dioxygenase Deficiency Disease?
Pronunciation: [hˈa͡ɪdɹəksɪfˌiːna͡ɪlpˌɪɹuːvˌe͡ɪt da͡ɪˈɒksɪd͡ʒənˌe͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Hydroxyphenylpyruvate Dioxygenase Deficiency Disease, also known as HPPD, is a rare genetic disorder that affects the metabolism of tyrosine, an amino acid. This condition is characterized by the diminished functioning of the enzyme hydroxyphenylpyruvate dioxygenase. Although the term HPPD is commonly used in scientific literature, it is helpful to know some synonyms to better understand this disorder. Some alternative names for HPPD include Tryptophan Pyruvate Aminotransferase Deficiency, Fumarylacetoacetase Deficiency, and Alpha-Ketoglutarate Dehydrogenase Deficiency. These synonyms highlight different aspects of the underlying metabolic processes affected in this disease. By knowing these alternatives, individuals can gain a more comprehensive understanding of this complex condition.
