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Summary Literature (0)
DOID:0060650 - dicarboxylic aminoaciduria

Disease Ontology Definition:An amino acid metabolic disorder that is characterized by an excess urinary excretion of aspartate and glutamate acidic amino acids.

Synonyms: glutamate-aspartate transport defect

Xenbase Genes : slc1a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009110 - dicarboxylic aminoaciduria

MIM:
MIM:222730 - DICARBOXYLIC AMINOACIDURIA; DCBXA

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a), autosomal recessive disease (is_a)