Calcium oxalate nephrolithiasis
Symptom Information:
Symptom ID: | HPO:0008672 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |