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Human Disease

3-methylglutaconic aciduria type 9

Term ID
DOID:0070002
Synonyms
  • 3-methylglutaconic acuduria type IX, MGCA9
Definition
A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/27573165
References
Ontology
Human Disease   ( DOID:0070002 )
Relationships
is a type of
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Genes Involved
Zebrafish Models