| Metadata | |
|---|---|
| ID | DOID:0060650 |
| Name | dicarboxylic aminoaciduria |
| Definition | An amino acid metabolic disorder that is characterized by an excess urinary excretion of aspartate and glutamate acidic amino acids. https://pubmed.ncbi.nlm.nih.gov/18200002/ |
| Xrefs |
SNOMEDCT_US_2023_03_01:716747007 |
| Subsets |
DO_rare_slim |
| Synonyms |
glutamate-aspartate transport defect [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |