Xanthine nephrolithiasis
Symptom Information:
Symptom ID: | HPO:0000804 | |||
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) Xanthine nephrolithiasis(HPO:0000804) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Hereditary xanthinuria | (Orphanet:3467) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
Xanthinuria type I | (Orphanet:93601) |