|OBO ID: DOID:0110001|
|Term Name:||3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome||Search Ontology:|
|Definition:||A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25. https://www.ncbi.nlm.nih.gov/pubmed/22683713|
|Ontology:||Human Disease (DOID:0110001)|
|is a type of:||
OTHER 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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