FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autoimmune lymphoproliferative syndrome type 2A ID (Ontology) DOID:0110115 (Human Disease)
Definition An autoimmune lymphoproliferative syndrome that has_material_basis_in mutation in the CASP10 gene.
Also Known As "ALPS2A" ; "autoimmune lymphoproliferative syndrome type IIA"
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 Genes
 autoimmune lymphoproliferative syndrome type 2A       1
 for disease ribbon | autoimmune lymphoproliferative syndrome type 2A       1
 model of | autoimmune lymphoproliferative syndrome type 2A       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_______________
hypersensitivity reaction type IV disease    |
 |__autoimmune lymphoproliferative syndrome__|
                                             autoimmune lymphoproliferative syndrome type 2A  1 rec.
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Is a autosomal dominant disease
autoimmune lymphoproliferative syndrome
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Synonyms
  • "ALPS2A" EXACT OMO:0003012
    "autoimmune lymphoproliferative syndrome type IIA" EXACT
Secondary IDs
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ICD10CM:D47.9
MESH:C565833
MIM:603909