OBO ID: DOID:0110737
Term Name: neurodegeneration with brain iron accumulation 3 Search Ontology:
Synonyms:
  • Adult basal ganglia disease
  • Ferritin-related neurodegeneration
  • Hereditary ferritinopathy
  • NBIA3
  • Neuroferritinopathy
  • Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset
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
References:
Ontology: Human Disease   ( DOID:0110737 )
Relationships
is a type of:
OTHER neurodegeneration with brain iron accumulation 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FTL Neurodegeneration with brain iron accumulation 3
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.