Just diagnosed with IgA glomerulonephritis?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees IgA glomerulonephritis, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive IgA glomerulonephritis hub →Overview
IgA glomerulonephritis is a rare condition. Also known as Berger disease, IgA nephropathy. Tomeko brings together the specialists, research, clinical trials, treatments and community for IgA glomerulonephritis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:34145 · ICD-10 N02 · GARD 0000863
Find care for IgA glomerulonephritis
Authoritative references for IgA glomerulonephritis
Research & market landscape for IgA glomerulonephritis
Following IgA glomerulonephritis for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for IgA glomerulonephritis — the real-world landscape behind the condition, in one place.
- Latest IgA glomerulonephritis research on PubMed ↗
- Recruiting IgA glomerulonephritis trials on ClinicalTrials.gov ↗
- Explore the IgA glomerulonephritis research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for IgA glomerulonephritis and every rare condition. See how Tomeko works with industry →
Common questions
What is IgA glomerulonephritis?
IgA glomerulonephritis is a rare condition. Also known as Berger disease, IgA nephropathy. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for IgA glomerulonephritis together in one place.
What are the symptoms of IgA glomerulonephritis?
Symptoms of IgA glomerulonephritis vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats IgA glomerulonephritis.
How is IgA glomerulonephritis treated?
Treatment for IgA glomerulonephritis depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see IgA glomerulonephritis, and review current options with them.
What causes IgA glomerulonephritis — is it genetic?
The cause and inheritance of IgA glomerulonephritis are described in the authoritative references linked on this page. A genetics or specialist clinician who treats IgA glomerulonephritis can explain what it means for you and your family.
I was just diagnosed with IgA glomerulonephritis — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees IgA glomerulonephritis, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for IgA glomerulonephritis?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat IgA glomerulonephritis, filtered to your area.
Are there clinical trials for IgA glomerulonephritis?
Tomeko shows live, recruiting studies for IgA glomerulonephritis from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Autosomal dominant distal renal tubular acidosis
- Autosomal dominant proximal renal tubular acidosis
- Autosomal dominant pseudohypoaldosteronism type 1
- Autosomal recessive distal renal tubular acidosis
- Autosomal recessive proximal renal tubular acidosis
- C3 glomerulonephritis
- Collagen type III glomerulopathy
- Complement 3 glomerulopathy