Hypouricemia
Symptom Information:
Symptom ID: | HPO:0003537 | ||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of nucleobase metabolism(HPO:0010932) Abnormality of purine metabolism(HPO:0004352) Decreased purine levels(HPO:0004369) Hypouricemia(HPO:0003537) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Purine and pyrimidine metabolism disorders(MedDRA:10037546) Disorders of purine metabolism(MedDRA:10070968) Hypouricemia(HPO:0003537) |
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Database Frequency: | 13 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Dent disease type 1 | (Orphanet:93622) |
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG | (OMIM:616026) |
Glycogen storage disease due to GLUT2 deficiency | (Orphanet:2088) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION | (OMIM:307830) |
HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY | (OMIM:242050) |
Hereditary renal hypouricemia | (Orphanet:94088) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Hypouricemia, renal, 2 | (OMIM:612076) |
Primary Fanconi syndrome | (Orphanet:3337) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |