Hyperuricemia

Symptom Information:

Symptom ID: HPO:0002149
Synonyms:
Hyperuricaemia [HPO:0002149]
Hyperuricemia (disorder) [Orphanet:49540]
Increased uric acid level (disorder) [Orphanet:49540]
HYPERURICAEMIA [HPO:0002149]
Hyperuricemia [Orphanet:49540]
Increased uric acid level [Orphanet:49540]
Hyperuricemia [OMIM:Hyperuricemia]
Uric acid level increased [Orphanet:49540]
Hyperuricaemia [Orphanet:49540]
Blood uric acid increased [MedDRA:10005861]
Blood urates increased [MedDRA:10005861]
Raised serum uric acid [MedDRA:10005861]
Urate high [MedDRA:10005861]
Urate increased [MedDRA:10005861]
Urates blood increased [MedDRA:10005861]
Uric acid blood increased [MedDRA:10005861]
Uric acid level increased [MedDRA:10005861]
Uric acid retention [MedDRA:10005861]
Uric acid high [MedDRA:10005861]
Uric acid increased [MedDRA:10005861]
Hyperuricaemia [MedDRA:10020903]
Hyperuricaemic [MedDRA:10020903]
Hyperuricemia [MedDRA:10020903]
Quality:
Cross references:
Orphanet:49540 "Hyperuricemia" [Orphanet:49540]
OMIM: "Hyperuricemia" [OMIM:Hyperuricemia]
UMLS:C0740394 "HYPERURICAEMIA" [HPO:0002149]
UMLS:C0740394 "Hyperuricemia" [Orphanet:49540]
UMLS:C0041981 "Increased uric acid level" [Orphanet:49540]
Is a (Direct Parents):
MedDRA Metabolism tests NEC
Orphanet Purine and pyrimidine metabolism disorders
HPO         Increased purine levels
MedDRA Disorders of purine metabolism
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)
                Increased purine levels(HPO:0004368)
                   Hyperuricemia(HPO:0002149)
MedDRA:
Investigations(MedDRA:10022891)
    Metabolic, nutritional and blood gas investigations(MedDRA:10027432)
       Metabolism tests NEC(MedDRA:10027434)
          Hyperuricemia(HPO:0002149)
Metabolism and nutrition disorders(MedDRA:10027433)
    Purine and pyrimidine metabolism disorders(MedDRA:10037546)
       Disorders of purine metabolism(MedDRA:10070968)
          Hyperuricemia(HPO:0002149)
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO (OMIM:102730)
Alström syndrome (Orphanet:64)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial juvenile hyperuricemic nephropathy type 1 (Orphanet:209886)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA (OMIM:609886)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Glycogen storage disease due to muscle phosphofructokinase deficiency (Orphanet:371)
HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE (OMIM:240000)
Hereditary fructose intolerance (Orphanet:469)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hyperuricemia - anemia - renal failure (Orphanet:217330)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Juvenile Paget disease (Orphanet:2801)
Kelley-Seegmiller syndrome (Orphanet:79233)
LACTIC ACIDOSIS, CHRONIC ADULT FORM (OMIM:150170)
LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT (OMIM:308950)
LESCH-NYHAN SYNDROME (OMIM:300322)
Lesch-Nyhan syndrome (Orphanet:510)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Renal cysts and diabetes syndrome (Orphanet:93111)
Sarcoidosis (Orphanet:797)
Thyrocerebrorenal syndrome (Orphanet:3327)
URATE OXIDASE, PSEUDOGENE (OMIM:191540)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1 (OMIM:138900)
[DEL] Uric acid concentration, serum, quantitative trait locus 4 (OMIM:612671)