Autoimmune Lymphoproliferative Syndrome
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.
推出的年份: 2010
树号: C15.604.515.138, C16.320.089, C20.111.288, C20.683.515.124
MeSH 单一 ID: D056735
进入的组:
Autoimmune Lymphoproliferative Syndromes
Lymphoproliferative Syndrome, Autoimmune
Lymphoproliferative Syndromes, Autoimmune
Syndrome, Autoimmune Lymphoproliferative
Syndromes, Autoimmune Lymphoproliferative
Canale-Smith Syndrome
Canale-Smith Syndromes
Syndrome, Canale-Smith
Syndromes, Canale-Smith
Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
Canale Smith Syndrome
Syndrome, Canale Smith
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 2B
Caspase-8 Deficiency
Caspase-8 Deficiencies
Deficiencies, Caspase-8
Deficiency, Caspase-8
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
Autoimmune Lymphoproliferative Syndrome, Type IIb
Caspase 8 Deficiency
Caspase 8 Deficiencies
Deficiencies, Caspase 8
Deficiency, Caspase 8
早前的内容:
Autoimmune Diseases (1997-2009)
Lymphoproliferative Disorders (1983-2009)
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