nephritis

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Information
Disease name
nephritis
Disease ID
DOID:10952
Description
"A kidney disease that is characterized by an inflammation of the kidneys." [url:https\://en.wikipedia.org/wiki/Nephritis]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04869462 Completed DS Titanium Ligation Clip in Urology (Prostatectomy and Nephrectomy) May 27, 2021 January 29, 2022
NCT00301613 Completed N/A Mycophenolate Mofetil (MMF) Versus Intravenous CTX Pulses in the Treatment of Adult Severe HSPN January 2003 January 2006
NCT00818948 Completed Phase 1 Safety Study of AMG 811 in Subjects With Systemic Lupus Erythematosus With and Without Glomerulonephritis March 2009 August 2014
NCT05686746 Recruiting Phase 2/Phase 3 Use of Baricitenib to Maintain of Remission June 1, 2022 August 1, 2023
NCT04387448 Terminated Phase 2 A Study of TRPC5 Channel Inhibitor in Patients With Diabetic Nephropathy, Focal Segmental Glomerulosclerosis, and Treatment-Resistant Minimal Change Disease July 28, 2020 November 1, 2022
NCT04950114 Terminated Phase 2 An Open-Label, Long-term Study of GFB-887 in Patients With Glomerular Kidney Diseases July 27, 2021 November 2, 2022
NCT01172002 Unknown status N/A Leflunomide Versus Azathioprine for Maintenance Therapy of Lupus Nephritis March 2010
NCT03884400 Withdrawn Distribution of Biospecimens From Biorepositories/Biobanks for Research Use January 1, 2021 March 1, 2026
NCT00508898 Withdrawn Phase 4 The Efficacy and Safety of Calcitriol for the Treatment of Lupus Nephritis and Persistent Proteinuria May 2008 September 2009
Disase is a (Disease Ontology)
DOID:557
Cross Reference ID (Disease Ontology)
ICD10CM:N08
Cross Reference ID (Disease Ontology)
MESH:D009393
Cross Reference ID (Disease Ontology)
NCI:C26833
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:52845002
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0027697
HPO alt_id (Human Phenotype Ontology)
HP:0008634
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0000123
MeSH unique ID (MeSH (Medical Subject Headings))
D009393