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DeCS
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Descriptor English:
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Autoimmune Lymphoproliferative Syndrome
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Descriptor Spanish:
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Síndrome Linfoproliferativo Autoinmune
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Descriptor Portuguese:
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Síndrome Linfoproliferativa Auto-Imune
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Synonyms English:
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Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
Canale Smith Syndrome
Caspase 8 Deficiency
Caspase-8 Deficiency
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Tree Number:
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C15.604.515.138
C16.320.089
C20.111.288
C20.683.515.124
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Definition English:
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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. |
See Related English:
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Antigens, CD95
Caspase 10
Caspase 8
Glucocorticoid-Induced TNFR-Related Protein
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History Note English:
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2010
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Allowable Qualifiers English:
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Record Number:
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53551
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Unique Identifier:
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D056735
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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