这个词是什么意思？
Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D056735 · MeSH 2026。
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