Glutaric aciduria

Symptom Information:

Symptom ID: HPO:0003150
Synonyms:
Glutaricaciduria [HPO:0003150]
Glutaric aciduria [OMIM:Glutaric aciduria]
Glutaricaciduria [OMIM:Glutaricaciduria]
Quality:
Cross references:
OMIM: "Glutaric aciduria" [OMIM:Glutaric aciduria]
OMIM: "Glutaricaciduria" [OMIM:Glutaricaciduria]
Is a (Direct Parents):
HPO         Dicarboxylic aciduria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Aciduria(HPO:0012072)
                      Organic aciduria(HPO:0001992)
                         Dicarboxylic aciduria(HPO:0003215)
                            Glutaric aciduria(HPO:0003150)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Organic aciduria(HPO:0001992)
                   Dicarboxylic aciduria(HPO:0003215)
                      Glutaric aciduria(HPO:0003150)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of dicarboxylic acid metabolism(HPO:0010995)
                Dicarboxylic aciduria(HPO:0003215)
                   Glutaric aciduria(HPO:0003150)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxy-3-methylglutaric aciduria (Orphanet:20)
D-2-hydroxyglutaric aciduria (Orphanet:79315)
Dilated cardiomyopathy with ataxia (Orphanet:66634)
Glutaric acidemia type 3 (Orphanet:35706)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)