Argininuria

Symptom Information:

Symptom ID: HPO:0003268
Synonyms:
Argininuria [OMIM:Argininuria]
Quality:
Cross references:
OMIM: "Argininuria" [OMIM:Argininuria]
Is a (Direct Parents):
HPO         Abnormality of arginine metabolism
HPO         Aminoaciduria
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)
                      Aminoaciduria(HPO:0003355)
                         Argininuria(HPO:0003268)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Argininuria(HPO:0003268)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Aminoaciduria(HPO:0003355)
                   Argininuria(HPO:0003268)
                Abnormality of glutamine family amino acid metabolism(HPO:0010902)
                   Abnormality of arginine metabolism(HPO:0010909)
                      Argininuria(HPO:0003268)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Argininemia (Orphanet:90)
Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Hyperdibasic aminoaciduria type 1 (Orphanet:1032)