Also known as ASPARTYLGLUCOSAMINIDASE DEFICIENCY, GLYCOSYLASPARAGINASE DEFICIENCY, aspartylglycosaminuria, Glycoasparaginase, Aga Deficiency, ASPARTYLGLUCOSAMINURIA; AGU, ASPARTYLGLUCOSAMINURIA
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Aspartylglucosaminuria (AGU) is an inherited disease that is characterized by a decline in mental functioning, accompanied by an increase in skin, bone and joint issues. AGU is a autosomal recessive disease.
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).