Glutaric Acidemia Type 3
Disease ID: disease_node_17501
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| Dbxref | GARD:12469, MIM:231690, ORDO:35706 |
|---|---|
| Subclassof | DOID_0050737, DOID_906 |
| Data Source | DOID |
| Synonyms | GA III, GA3, glutaric aciduria 3, glutaric aciduria III, glutaric aciduria type 3, glutaryl-CoA oxidase deficiency |
| Doid Label | glutaric acidemia type 3 |
| Doid Description | 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17501 |
| Doid Id | DOID_0112246 |
| Label | Glutaric Acidemia Type 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Peroxisomal Disorders(ID:disease_node_9830) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)