FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term neurodegeneration with brain iron accumulation 3 ID (Ontology) DOID:0110737 (Human Disease)
Definition A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33.
Also Known As "Adult basal ganglia disease" ; "Ferritin-related neurodegeneration" ; "Hereditary ferritinopathy" (for all, see Synonyms field below)
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 neurodegeneration with brain iron accumulation 3       3
 for disease ribbon | neurodegeneration with brain iron accumulation 3       3
 model of | neurodegeneration with brain iron accumulation 3       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease______________________
neurodegenerative disease                           |
 |__neurodegeneration with brain iron accumulation__|
                                                    neurodegeneration with brain iron accumulation 3  3 rec.
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Is a autosomal dominant disease
neurodegeneration with brain iron accumulation
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Synonyms
  • "Adult basal ganglia disease" EXACT
    "Ferritin-related neurodegeneration" EXACT
    "Hereditary ferritinopathy" EXACT
    "NBIA3" EXACT OMO:0003012
    "Neuroferritinopathy" EXACT
    "Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset" EXACT
Secondary IDs
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MESH:C548080
MIM:606159
ORDO:157846
SNOMEDCT_US_2023_03_01:699299001
UMLS_CUI:C1853578