has material basis in germline mutation in FTL neuroferritinopathy https://www.malacards.org/card/neurodegeneration_with_brain_iron_accumulation_3 hereditary ferritinopathy NANDO:1200539 adult basal ganglia disease DOID:0110737 neurodegeneration with brain iron accumulation 3 Editor note: consider relation to basal ganglia ICD9:333.0 GARD:0010686 NBIA3 Neuroferritinopathy is a late-onset type of neurodegeneration with brain iron accumulation (NBIA) characterized by progressive chorea or dystonia and subtle cognitive deficits. OMIM:606159 basal ganglia disease adult-onset UMLS:C1853578 MESH:C548080 SCTID:699299001 neuroferritinopathy ferritin-related neurodegeneration neurodegeneration with brain iron accumulation type 3 MEDGEN:381211 Orphanet:157846 MONDO:0011638 NANDO:1200542 Huntington disease-like syndrome disorder of iron metabolism and transport neurodegeneration with brain iron accumulation