Hyperuricemia
Symptom Information:
Symptom ID: | HPO:0002149 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Increased purine levels(HPO:0004368) Hyperuricemia(HPO:0002149) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Purine and pyrimidine metabolism disorders(MedDRA:10037546) Disorders of purine metabolism(MedDRA:10070968) Hyperuricemia(HPO:0002149) Investigations(MedDRA:10022891) Metabolic, nutritional and blood gas investigations(MedDRA:10027432) Metabolism tests NEC(MedDRA:10027434) Hyperuricemia(HPO:0002149) |
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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) |