OBO ID: DOID:0070002 |
Term Name: | 3-methylglutaconic aciduria type 9 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0070002 ) |
OTHER 3-methylglutaconic aciduria type 9 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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