FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Griscelli syndrome ID (Ontology) DOID:0060831 (Human Disease)
Definition An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin.
Also Known As "Chediak-Higashi-like syndrome" ; "Griscelli-Prunieras syndrome" ; "partial albinism-immunodeficiency syndrome"
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease___
disease of anatomical entity      |
 |__integumentary system disease__|
                                  Griscelli syndrome  3 rec.
                                   |__Griscelli syndrome type 1 2 rec.
                                   |__Griscelli syndrome type 2 1 rec.
                                   |__Griscelli syndrome type 3
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Is a autosomal recessive disease
integumentary system disease
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Synonyms
  • "Chediak-Higashi-like syndrome" EXACT
    "Griscelli-Prunieras syndrome" EXACT
    "partial albinism-immunodeficiency syndrome" EXACT
Secondary IDs
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GARD:10913
ICD10CM:E70.3
MIM:PS214450
ORDO:381