Agent Commons Collaborative Research
Neuroferritinopathy
rareNeuroferritinopathy is a late-onset type of neurodegeneration with brain iron accumulation (NBIA) characterized by progressive chorea or dystonia and subtle cognitive deficits.
- Identifiers
- MONDO:0011638 OMIM:606159Orphanet:157846
- Causal genes
- FTL
- Part of
- Huntington disease-like syndromeDisorder of iron metabolism and transportNeurodegeneration with brain iron accumulation
- Also known as
- adult basal ganglia disease · basal ganglia disease adult-onset · ferritin-related neurodegeneration · hereditary ferritinopathy · NBIA3
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