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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Glycosuria
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Accession:DOID:9003426 term browser browse the term
Definition:The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA).
Synonyms:exact_synonym: glucosuria
 primary_id: MESH:D006029;   RDO:0005686
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
cataract 47 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G SLC16A12 solute carrier family 16 member 12 IAGP ClinVar Annotator: match by term: CATARACT, JUVENILE, WITH MICROCORNEA ClinVar
OMIM
PMID:17458810, PMID:18304496, PMID:21778275, PMID:26376857 NCBI chr10:89,430,299...89,536,029
Ensembl chr10:89,430,299...89,556,641
JBrowse link
renal glycosuria term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G HNRNPF heterogeneous nuclear ribonucleoprotein F ISS OMIM:233100 MouseDO NCBI chr10:43,385,618...43,409,186
Ensembl chr10:43,385,617...43,409,166
JBrowse link
G RUSF1 RUS family member 1 IAGP ClinVar Annotator: match by term: Glycosuria, Renal ClinVar PMID:14569097, PMID:14614622, PMID:15110322, PMID:18622023, PMID:28492532 NCBI chr16:31,489,475...31,508,391
Ensembl chr16:31,489,471...31,509,309
JBrowse link
G SLC5A2 solute carrier family 5 member 2 IAGP DNA:frameshift mutation, missense mutation:cds:p.Q167fsX186, p.N654S (human)
ClinVar Annotator: match by term: Glycosuria, Renal
DNA:nonsense mutation:cds:p.W440X (human)
ClinVar
OMIM
PMID:12436245, PMID:14569097, PMID:14614622, PMID:15110322, PMID:18622023, PMID:21165652, PMID:25741868, PMID:26376857, PMID:28492532, PMID:14614622, PMID:12436245 RGD:1599049, RGD:737731 NCBI chr16:31,482,535...31,490,769
Ensembl chr16:31,483,002...31,490,860
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17777
    Nutritional and Metabolic Diseases 4967
      disease of metabolism 4967
        glucose metabolism disease 1593
          Glycosuria 4
            renal glycosuria + 4
Path 2
Term Annotations click to browse term
  disease 17777
    Nutritional and Metabolic Diseases 4967
      disease of metabolism 4967
        acquired metabolic disease 3111
          carbohydrate metabolism disease 1593
            glucose metabolism disease 1593
              Glycosuria 4
                renal glycosuria + 4
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.