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DO Term : neurodegeneration with brain iron accumulation 4 [DOID:0110738] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12.

synonyms:
NBIA due to C19orf12 mutation,
MPAN,
OMIM:614298,
ORDO:289560,
Neurodegeneration with brain iron accumulation type 4,
NBIA4,
ICD10CM:G23.0,
Mitochondrial Protein-Associated Neurodegeneration,
Neurodegeneration with brain iron accumulation due to C19orf12 mutation,
614298

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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