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 3 ID (Ontology) DOID:0110119 (Human Disease)
Definition An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the PRKCD gene on chromosome 3p21.
Also Known As "ALPS3" ; "autoimmune lymphoproliferative syndrome type III"
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 Genes
 autoimmune lymphoproliferative syndrome type 3       1
 for disease ribbon | autoimmune lymphoproliferative syndrome type 3       1
 model of | autoimmune lymphoproliferative syndrome type 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease______________
hypersensitivity reaction type IV disease    |
 |__autoimmune lymphoproliferative syndrome__|
                                             autoimmune lymphoproliferative syndrome type 3  1 rec.
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Is a autosomal recessive disease
autoimmune lymphoproliferative syndrome
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Synonyms
  • "ALPS3" EXACT OMO:0003012
    "autoimmune lymphoproliferative syndrome type III" EXACT
Secondary IDs
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MIM:615559