OBO ID: DOID:0110001 |
Term Name: | 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0110001 ) |
OTHER 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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