Glycosuria

Symptom Information:

Symptom ID: HPO:0003076
Synonyms:
Glucosuria [HPO:0003076]
Glucosuria [OMIM:Glucosuria]
Glycosuria [OMIM:Glycosuria]
Glycosuria (less common) [OMIM:Glycosuria (less common)]
Glycosuria [MedDRA:10018473]
Quality:
Cross references:
OMIM: "Glucosuria" [OMIM:Glucosuria]
OMIM: "Glycosuria" [OMIM:Glycosuria]
OMIM: "Glycosuria (less common)" [OMIM:Glycosuria (less common)]
UMLS:C0017979 "Glucosuria" [HPO:0003076]
Is a (Direct Parents):
HPO         Abnormality of urine glucose concentration
MedDRA Urinary abnormalities
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Abnormality of urine glucose concentration(HPO:0011016)
                Glycosuria(HPO:0003076)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Abnormality of urine glucose concentration(HPO:0011016)
                   Glycosuria(HPO:0003076)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Abnormality of urine glucose concentration(HPO:0011016)
                      Glycosuria(HPO:0003076)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Glycosuria(HPO:0003076)
Database Frequency: 32 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY (OMIM:210550)
Bardet-Biedl syndrome 12 (OMIM:615989)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cystinosis (Orphanet:213)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
FANCONI RENOTUBULAR SYNDROME 3 (OMIM:615605)
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG (OMIM:616026)
Fabry disease (Orphanet:324)
Fanconi renotubular syndrome 1 (OMIM:134600)
GLUCOGLYCINURIA (OMIM:138070)
Glucose-galactose malabsorption (Orphanet:35710)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary fructose intolerance (Orphanet:469)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
Isolated cytochrome C oxidase deficiency (Orphanet:254905)
Juvenile cataract - microcornea - renal glucosuria (Orphanet:247794)
Maturity-onset diabetes of the young, type 3 (OMIM:600496)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (OMIM:308990)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Pearson syndrome (Orphanet:699)
Primary Fanconi syndrome (Orphanet:3337)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal glucosuria (Orphanet:69076)
Tyrosinemia type 1 (Orphanet:882)
Wilson disease (Orphanet:905)