FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary spherocytosis type 3 ID (Ontology) DOID:0110918 (Human Disease)
Definition A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1.
Also Known As "hereditary spherocytosis 3" ; "HS3" ; "SPH3"
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 Genes
 hereditary spherocytosis type 3       1
 for disease ribbon | hereditary spherocytosis type 3       1
 model of | hereditary spherocytosis type 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
congenital hemolytic anemia      |
 |__hereditary spherocytosis_____|
                                 hereditary spherocytosis type 3  1 rec.
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Is a autosomal recessive disease
hereditary spherocytosis
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Synonyms
  • "hereditary spherocytosis 3" EXACT
    "HS3" EXACT OMO:0003012
    "SPH3" EXACT OMO:0003012
Secondary IDs
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MIM:270970