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Langerhans cell histiocytosis

Just diagnosed with Langerhans cell histiocytosis?

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

Open the full Langerhans cell histiocytosis hub →

Overview

Langerhans cell histiocytosis is a rare condition. Also known as Histiocytosis X, Langerhans cell granulomatosis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Langerhans cell histiocytosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:389 · OMIM 604856 · ICD-10 C96.0, C96.5, C96.6 · GARD 0006858

Find care for Langerhans cell histiocytosis

Authoritative references for Langerhans cell histiocytosis

Common questions

I was just diagnosed with Langerhans cell histiocytosis — what should I do first?

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

Where can I find a specialist for Langerhans cell histiocytosis?

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

Are there clinical trials for Langerhans cell histiocytosis?

Tomeko shows live, recruiting studies for Langerhans cell histiocytosis 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