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Date: Tue Jan 28 2025
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glutaric acidemia type 3
DOID:0112246
Summary
Associated Genes
Associated Alleles
Associated Models
Disease
glutaric acidemia type 3
Definition
A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the SUGCT gene on chromosome 7p14.1.
[1]
Synonyms
GA III
GA3
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Cross References
GARD:12469
MIM:231690
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Parent Terms
autosomal recessive disease
peroxisomal disease
Child Terms
None
Sources of Associations
RGD
MGI
ZFIN
FB
WB
SGD
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