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Infantile nephronophthisis

Just diagnosed with Infantile nephronophthisis?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Infantile nephronophthisis, look for clinical trials, and connect with others living with it — all in one place.

Open the full Infantile nephronophthisis hub →

Overview

Infantile nephronophthisis is a rare condition. Also known as Autosomal recessive infantile NPHP, Autosomal recessive infantile nephronophthisis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Infantile nephronophthisis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:93591 · OMIM 602088, 615382 · ICD-10 Q61.5 · GARD 0018182

Find care for Infantile nephronophthisis

Authoritative references for Infantile nephronophthisis

Common questions

I was just diagnosed with Infantile nephronophthisis — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Infantile nephronophthisis, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Infantile nephronophthisis?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Infantile nephronophthisis, filtered to your area.

Are there clinical trials for Infantile nephronophthisis?

Tomeko shows live, recruiting studies for Infantile nephronophthisis from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com