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syndróm autoimunitný lymfoproliferatívny
Record number d056735 Date 06.06.2025 Type M - MESH Topical term syndróm autoimunitný lymfoproliferatívny Other term English (Pseudonym) Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
English (Pseudonym) Autoimmune Lymphoproliferative Syndrome Type 2B
English (Pseudonym) Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
English (Pseudonym) Canale Smith Syndrome
English (Pseudonym) Caspase 8 Deficiency
English (Pseudonym) Caspase-8 Deficiency
Slovak (Pseudonym) syndróm autoimunitný lymfoproliferatívny, typ 1, autozomálne dominantný
syndróm autoimunitný lymfoproliferatívny, typ 2B
Slovak (Pseudonym) syndróm autoimunitný lymfoproliferatívny, typ 2B (ALPS2B)
Slovak (Pseudonym) Canale Smithov syndróm
Slovak (Pseudonym) Canalovej Smithov syndróm
Slovak (Pseudonym) deficit kaspázy 8
See also (Later heading) receptor fas
(Later heading) kaspáza 8
(Later heading) proteín príbuzný TNFR, indukovaný glukokortikoidmi
(Later heading) kaspáza 10
(Skutočné meno) receptor fas
(Skutočné meno) kaspáza 8
(Skutočné meno) proteín príbuzný TNFR, indukovaný glukokortikoidmi
(Skutočné meno) kaspáza 10
UDC C15.604.515.138C16.320.089C20.111.288C20.683.515.124 Note 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. 
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Number of the records: 1