Calcium oxalate nephrolithiasis

Symptom Information:

Symptom ID: HPO:0008672
Synonyms:
Calcium oxalate urolithiasis [HPO:0008672]
Oxalate nephrolithiasis [HPO:0008672]
Calcium oxalate nephrolithiasis [OMIM:Calcium oxalate nephrolithiasis]
Oxalate nephrolithiasis [OMIM:Oxalate nephrolithiasis]
Quality:
Cross references:
OMIM: "Calcium oxalate nephrolithiasis" [OMIM:Calcium oxalate nephrolithiasis]
OMIM: "Oxalate nephrolithiasis" [OMIM:Oxalate nephrolithiasis]
Is a (Direct Parents):
HPO         Calcium nephrolithiasis
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 upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Nephrolithiasis(HPO:0000787)
                         Calcium nephrolithiasis(HPO:0004724)
                            Calcium oxalate nephrolithiasis(HPO:0008672)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

5-oxoprolinase deficiency (Orphanet:33572)
HYPERCALCIURIA, ABSORPTIVE, 2 (OMIM:143870)
HYPERGLYCINURIA (OMIM:138500)
Idiopathic hypercalciuria (Orphanet:2197)
NEPHROLITHIASIS, CALCIUM OXALATE (OMIM:167030)
Primary Fanconi syndrome (Orphanet:3337)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Primary hyperoxaluria type 2 (Orphanet:93599)
Primary hyperoxaluria type 3 (Orphanet:93600)