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neurodegeneration with brain iron accumulation 3
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http://purl.obolibrary.org/obo/DOID_0110737
A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
neurodegeneration with brain iron accumulation 3
Synonyms
- Adult basal ganglia disease
- Ferritin-related neurodegeneration
- Hereditary ferritinopathy
- NBIA3
- Neuroferritinopathy
- Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset
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disease_ontology
id
DOID:0110737