FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Gaucher's disease type III ID (Ontology) DOID:0110959 (Human Disease)
Definition A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22.
Also Known As "Gaucher Disease, Chronic Neuronopathic Type" ; "Gaucher Disease, Juvenile And Adult, Cerebral" ; "Gaucher Disease, Subacute Neuronopathic Type" (for all, see Synonyms field below)
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 Genes
 Gaucher's disease type III       2
 for disease ribbon | Gaucher's disease type III       2
 model of | Gaucher's disease type III       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
sphingolipidosis                 |
 |__Gaucher's disease____________|
                                 Gaucher's disease type III  2 rec.
                                  |__Gaucher's disease type IIIC 2 rec.
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Is a autosomal recessive disease
Gaucher's disease
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Synonyms
  • "Gaucher Disease, Chronic Neuronopathic Type" EXACT
    "Gaucher Disease, Juvenile And Adult, Cerebral" EXACT
    "Gaucher Disease, Subacute Neuronopathic Type" EXACT
    "GD III" EXACT OMO:0003012
Secondary IDs
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ICD10CM:E75.2
MIM:231000
ORDO:77261