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DO Term : 3-methylglutaconic aciduria type 9 [DOID:0070002] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13.

synonyms:
617698,
OMIM:617698,
3-methylglutaconic acuduria type IX, MGCA9

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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