FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term 3-methylglutaconic aciduria type 9 ID (Ontology) DOID:0070002 (Human Disease)
Definition A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13.
Also Known As "3-methylglutaconic acuduria type IX, MGCA9"
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 Genes
 3-methylglutaconic aciduria type 9       3
 for disease ribbon | 3-methylglutaconic aciduria type 9       3
 model of | 3-methylglutaconic aciduria type 9       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
organic acidemia                 |
 |__3-methylglutaconic aciduria__|
                                 3-methylglutaconic aciduria type 9  3 rec.
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Is a autosomal recessive disease
3-methylglutaconic aciduria
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Synonyms
  • "3-methylglutaconic acuduria type IX, MGCA9" EXACT
Secondary IDs
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MIM:617698