Disease

3-methylglutaconic aciduria type 1

Name: 3-methylglutaconic aciduria type 1
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110002 3-methylglutaconic aciduria type 1 A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22. 3MG-CoA hydratase deficiency 3-methylglutaconic aciduria type I 3-methylglutaconyl-CoA hydratase deficiency MGA1 MGA type I

Definition

A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22.

Synonyms

3-methylglutaconic aciduria type I
3-methylglutaconyl-CoA hydratase deficiency

Cross References

MESH:C562801
MIM:250950

Parent Terms

3-methylglutaconic aciduria
autosomal recessive disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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