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An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D007619 · MeSH 2026。
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