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3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (DOID:0110001)
Synonyms: 3-methylglutaconic aciduria type 6; MEGDEL; MEGDEL syndrome; MGCA6
Alt IDs: OMIM:614739, ICD10CM:E71.1, ORDO:352328
Definition: A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the SERAC1 gene on chromosome 6q25.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/12/2017
MGI 6.10
The Jackson Laboratory