BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
rs3825942
,
CYP51
,
Metabolism of xenobiotics
,
Diabetes mellitus
,
Lung
,
Doxorubicin
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
Xanthinuria
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
OMIM - Xanthinuria
Mouse Phenotypes - Metabolic disease
OMIM - Molybdenum cofactor deficiency
Explore Curated Studies Results
Literature
Most Relevant Literature
Candidate causative variant for xanthinuria in a Domestic Shorthair cat.
Fortuitous Discovery of Hereditary Xanthinuria.
Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function…
Xanthinuria secondary to allopurinol treatment in dogs with leishmaniosis: Current perspectives of t…
A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
A Safety and Efficacy Study of SHR4640 and Febuxostat in Subjects With Hyperuricemia
The Drug-Drug Interaction of SHR4640 and Febuxostat in Patients With Hyperuricemia
Phase 3, Febuxostat, Allopurinol and Placebo-Controlled Study in Gout Subjects.
The Drug-Drug Interaction of SHR4640, Febuxostat and Colchicine in Patients With Gout
Tranilast Plus Allopurinol in Patients With Moderate to Severe Gout (TAnGO)
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ