这个词是什么意思？
An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D003555 · MeSH 2026。
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