Gout

Symptom Information:

Symptom ID: HPO:0001997
Synonyms:
Gouty arthritis [HPO:0001997]
Gout [OMIM:Gout]
Gouty arthritis [OMIM:Gouty arthritis]
Gouty arthritis [MedDRA:10018634]
Gout [MedDRA:10018627]
Quality:
Cross references:
OMIM: "Gout" [OMIM:Gout]
OMIM: "Gouty arthritis" [OMIM:Gouty arthritis]
UMLS:C0018099 "Gout" [HPO:0001997]
Is a (Direct Parents):
HPO         Arthritis
HPO         Hyperuricemia
MedDRA Disorders of purine metabolism
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Arthritis(HPO:0001369)
                   Gout(HPO:0001997)
       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)
                      Gout(HPO:0001997)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Purine and pyrimidine metabolism disorders(MedDRA:10037546)
       Disorders of purine metabolism(MedDRA:10070968)
          Gout(HPO:0001997)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Familial juvenile hyperuricemic nephropathy type 1 (Orphanet:209886)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
GLYCOPROTEIN STORAGE DISEASE (OMIM:232900)
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)
Kelley-Seegmiller syndrome (Orphanet:79233)
LESCH-NYHAN SYNDROME (OMIM:300322)
Lesch-Nyhan syndrome (Orphanet:510)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Renal cysts and diabetes syndrome (Orphanet:93111)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] Uric acid concentration, serum, quantitative trait locus 4 (OMIM:612671)