| Metadata | |
|---|---|
| ID | DOID:0110737 |
| Name | neurodegeneration with brain iron accumulation 3 |
| 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. https://www.ncbi.nlm.nih.gov/pubmed/16116125 |
| Xrefs |
SNOMEDCT_US_2023_03_01:699299001 |
| Subsets |
DO_rare_slim |
| Synonyms |
Adult basal ganglia disease [EXACT] Ferritin-related neurodegeneration [EXACT] Hereditary ferritinopathy [EXACT] NBIA3 [EXACT] Neuroferritinopathy [EXACT] Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |