FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dicarboxylic aminoaciduria ID (Ontology) DOID:0060650 (Human Disease)
Definition An amino acid metabolic disorder that is characterized by an excess urinary excretion of aspartate and glutamate acidic amino acids.
Also Known As "glutamate-aspartate transport defect"
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DO.org
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 Genes
 dicarboxylic aminoaciduria       1
 for disease ribbon | dicarboxylic aminoaciduria       1
 model of | dicarboxylic aminoaciduria       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease____
inherited metabolic disorder       |
 |__amino acid metabolic disorder__|
                                   dicarboxylic aminoaciduria  1 rec.
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Is a autosomal recessive disease
amino acid metabolic disorder
Part of
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Synonyms
  • "glutamate-aspartate transport defect" EXACT
Secondary IDs
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GARD:1855
MESH:C536171
MIM:222730
ORDO:2195
SNOMEDCT_US_2023_03_01:716747007
UMLS_CUI:C1857253