Hydroxyprolinuria

Symptom Information:

Symptom ID: HPO:0003080
Synonyms:
Elevated urinary hydroxyproline [HPO:0003080]
Elevated urinary hydroxyproline [OMIM:Elevated urinary hydroxyproline]
Hydroxyprolinuria [OMIM:Hydroxyprolinuria]
Hydroxyprolinuria [MedDRA:10053122]
Quality:
Cross references:
OMIM: "Elevated urinary hydroxyproline" [OMIM:Elevated urinary hydroxyproline]
OMIM: "Hydroxyprolinuria" [OMIM:Hydroxyprolinuria]
UMLS:C0948585 "Hydroxyprolinuria" [HPO:0003080]
Is a (Direct Parents):
HPO         Aminoaciduria
MedDRA Urinary abnormalities
HPO         Abnormality of proline metabolism
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)
                         Hydroxyprolinuria(HPO:0003080)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Abnormality of glutamine family amino acid metabolism(HPO:0010902)
                   Abnormality of proline metabolism(HPO:0010907)
                      Hydroxyprolinuria(HPO:0003080)
                Aminoaciduria(HPO:0003355)
                   Hydroxyprolinuria(HPO:0003080)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Hydroxyprolinuria(HPO:0003080)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Hydroxyprolinuria(HPO:0003080)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

BRUCK SYNDROME 2 (OMIM:609220)
Familial expansile osteolysis (Orphanet:85195)
Hyperprolinemia type 1 (Orphanet:419)
Hyperprolinemia type 2 (Orphanet:79101)
Iminoglycinuria (Orphanet:42062)
Juvenile Paget disease (Orphanet:2801)
PAGET DISEASE OF BONE (OMIM:602080)