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 5 ID (Ontology) DOID:0110920 (Human Disease)
Definition A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2.
Also Known As "hereditary spherocytosis 5" ; "HS5" ; "SPH5"
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 Genes
 hereditary spherocytosis type 5       1
 for disease ribbon | hereditary spherocytosis type 5       1
 model of | hereditary spherocytosis type 5       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
congenital hemolytic anemia      |
 |__hereditary spherocytosis_____|
                                 hereditary spherocytosis type 5  1 rec.
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Is a autosomal recessive disease
hereditary spherocytosis
Part of
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Synonyms
  • "hereditary spherocytosis 5" EXACT
    "HS5" EXACT OMO:0003012
    "SPH5" EXACT OMO:0003012
Secondary IDs
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MIM:612690