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Primary intestinal lymphangiectasia

Just diagnosed with Primary intestinal lymphangiectasia?

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

Open the full Primary intestinal lymphangiectasia hub →

Overview

Primary intestinal lymphangiectasia is a rare condition. Also known as Waldmann disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Primary intestinal lymphangiectasia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:90362 · OMIM 152800 · ICD-10 I89.0 · GARD 0007873

Find care for Primary intestinal lymphangiectasia

Authoritative references for Primary intestinal lymphangiectasia

Common questions

I was just diagnosed with Primary intestinal lymphangiectasia — what should I do first?

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

Where can I find a specialist for Primary intestinal lymphangiectasia?

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

Are there clinical trials for Primary intestinal lymphangiectasia?

Tomeko shows live, recruiting studies for Primary intestinal lymphangiectasia 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