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What is another word for Inborn Amino Acidopathies?

Pronunciation: [ˈɪnbɔːn ɐmˈiːnə͡ʊ ɐsɪdˈɒpəθɪz] (IPA)

Inborn Amino Acidopathies, also known as inborn errors of metabolism, are a group of genetic disorders that affect the way the body breaks down amino acids. They result from defects in enzymes responsible for the metabolism of these essential molecules. Inborn Amino Acidopathies can lead to a wide range of symptoms, including intellectual disability, developmental delay, seizures, and organ dysfunction. Synonyms for this medical condition include inborn errors of amino acid metabolism, congenital aminoacidopathies, and genetic amino acid disorders. These alternative terms help clinicians and researchers communicate effectively, facilitating diagnostic processes, treatment decisions, and discussions with patients and their families.
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What are the opposite words for Inborn Amino Acidopathies?

Antonyms for the term "inborn amino acidopathies" can be terms like acquired, developed, or late-onset. Inborn amino acidopathies are a group of rare genetic disorders that affect the body's ability to break down certain amino acids properly. This can lead to a buildup of toxic substances in the body, resulting in a host of developmental, neurological, metabolic, and other health problems. Conversely, acquired amino acidopathies can result from exposure to toxic substances or from the use of certain drugs or medicines. Unlike inborn amino acidopathies, these conditions can develop later in life and are not genetic in nature. Late-onset amino acidopathies can also present with similar symptoms but occur later in life.

What are the antonyms for Inborn amino acidopathies?

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