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Hereditary fructosuria

Just diagnosed with Hereditary fructosuria?

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

Open the full Hereditary fructosuria hub →

Overview

Hereditary fructosuria is a rare condition. Also known as Hereditary fructose-1-phosphate aldolase deficiency, Hereditary fructosemia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary fructosuria so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:469 · OMIM 229600 · ICD-10 E74.1 · GARD 0006622

Find care for Hereditary fructosuria

Authoritative references for Hereditary fructosuria

Common questions

I was just diagnosed with Hereditary fructosuria — what should I do first?

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

Where can I find a specialist for Hereditary fructosuria?

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

Are there clinical trials for Hereditary fructosuria?

Tomeko shows live, recruiting studies for Hereditary fructosuria 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