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 4 ID (Ontology) DOID:0110117 (Human Disease)
Definition An autoimmune lymphoproliferative syndrome that has_material_basis_in somatic mutation in the NRAS gene or the KRAS gene on chromosome 12p12.
Also Known As "ALPS type 4" ; "ALPS type IV" ; "ALPS4" (for all, see Synonyms field below)
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 Genes
 autoimmune lymphoproliferative syndrome type 4       1
 for disease ribbon | autoimmune lymphoproliferative syndrome type 4       1
 model of | autoimmune lymphoproliferative syndrome type 4       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease_______________
hypersensitivity reaction type IV disease    |
 |__autoimmune lymphoproliferative syndrome__|
                                             autoimmune lymphoproliferative syndrome type 4  1 rec.
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Is a autosomal dominant disease
autoimmune lymphoproliferative syndrome
Part of
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Synonyms
  • "ALPS type 4" EXACT
    "ALPS type IV" EXACT
    "ALPS4" EXACT OMO:0003012
    "autoimmune lymphoproliferative syndrome type IV" EXACT
    "RALD" EXACT OMO:0003012
    "RAS-associated autoimmune leukoproliferative disease" EXACT
    "RAS-associated autoimmune leukoproliferative disorder" EXACT
Secondary IDs
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ICD10CM:D72.8
MIM:614470
ORDO:268114