Hypouricemia

Symptom Information:

Symptom ID: HPO:0003537
Synonyms:
Hypouricaemia [HPO:0003537]
Hypouricemia [OMIM:Hypouricemia]
Hypouricaemia [MedDRA:10021131]
Quality:
Cross references:
OMIM: "Hypouricemia" [OMIM:Hypouricemia]
UMLS:C0221333 "Hypouricaemia" [HPO:0003537]
Is a (Direct Parents):
MedDRA Disorders of purine metabolism
HPO         Decreased purine levels
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)
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)