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DO Term : neurodegeneration with brain iron accumulation 3 [DOID:0110737] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33.

synonyms:
NBIA3,
MESH:C548080,
Hereditary ferritinopathy,
Neuroferritinopathy,
OMIM:606159,
Adult basal ganglia disease,
Ferritin-related neurodegeneration,
ORDO:157846,
Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset,
UMLS_CUI:C1853578,
606159,
SNOMEDCT_US_2023_03_01:699299001

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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