What is another word for Alpha Aminoadipic Semialdehyde Deficiency Disease?
Pronunciation: [ˈalfəɹ ɐmˌɪnə͡ʊdˈɪpɪk sˌɛmɪˈaldɪhˌa͡ɪd dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Alpha aminoadipic semialdehyde deficiency disease is a rare genetic disorder that affects the metabolism of amino acids. This condition is caused by a deficiency in the enzyme aminoadipic semialdehyde dehydrogenase, which leads to a buildup of aminoadipic semialdehyde in the body. This can result in various symptoms such as developmental delays, seizures, intellectual disability, and abnormal urine odor. Although there are no exact synonyms for this specific disorder, it falls under the category of organic acidurias, which are a group of inherited metabolic disorders characterized by the accumulation of organic acids in the body.
