Dicarboxylic aciduria

Symptom Information:

Symptom ID: HPO:0003215
Synonyms:
Dicarboxylic aciduria [OMIM:Dicarboxylic aciduria]
Quality:
Cross references:
OMIM: "Dicarboxylic aciduria" [OMIM:Dicarboxylic aciduria]
Is a (Direct Parents):
HPO         Abnormality of dicarboxylic acid metabolism
HPO         Organic aciduria
HPO         L-2-hydroxyglutaric aciduria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of dicarboxylic acid metabolism(HPO:0010995)
                Dicarboxylic aciduria(HPO:0003215)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Organic aciduria(HPO:0001992)
                   Dicarboxylic aciduria(HPO:0003215)
       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)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (Orphanet:71212)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
RIBOFLAVIN DEFICIENCY (OMIM:615026)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)