About   Help   FAQ
Disease Ontology Browser
neurodegeneration with brain iron accumulation 3 (DOID:0110737)
Synonyms: Adult basal ganglia disease; Ferritin-related neurodegeneration; Hereditary ferritinopathy; NBIA3; Neuroferritinopathy; Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset
Alt IDs: OMIM:606159, ICD10CM:G23.0, MESH:C548080, ORDO:157846, UMLS_CUI:C1853578
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/15/2017
MGI 6.10
The Jackson Laboratory