Prolinuria

Symptom Information:

Symptom ID: HPO:0003137
Synonyms:
Prolinuria [OMIM:Prolinuria]
Quality:
Cross references:
OMIM: "Prolinuria" [OMIM:Prolinuria]
UMLS:C0268534 "Prolinuria" [HPO:0003137]
Is a (Direct Parents):
HPO         Aminoaciduria
HPO         Abnormality of proline metabolism
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Prolinuria(HPO:0003137)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Aminoaciduria(HPO:0003355)
                   Prolinuria(HPO:0003137)
                Abnormality of glutamine family amino acid metabolism(HPO:0010902)
                   Abnormality of proline metabolism(HPO:0010907)
                      Prolinuria(HPO:0003137)
       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)
                         Prolinuria(HPO:0003137)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

5-oxoprolinase deficiency (Orphanet:33572)
Hyperprolinemia type 1 (Orphanet:419)
Hyperprolinemia type 2 (Orphanet:79101)
Iminoglycinuria (Orphanet:42062)