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Neutral lipid storage myopathy

Just diagnosed with Neutral lipid storage myopathy?

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

Open the full Neutral lipid storage myopathy hub →

Overview

Neutral lipid storage myopathy is a rare condition. Also known as Adipose triglyceride lipase deficiency, NLSDM, Neutral lipid storage disease type M, Neutral lipid storage disease with myopathy without ichthyosis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Neutral lipid storage myopathy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:98908 · OMIM 610717 · ICD-10 E75.5 · GARD 0010288

Find care for Neutral lipid storage myopathy

Authoritative references for Neutral lipid storage myopathy

Common questions

I was just diagnosed with Neutral lipid storage myopathy — what should I do first?

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

Where can I find a specialist for Neutral lipid storage myopathy?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Neutral lipid storage myopathy, filtered to your area.

Are there clinical trials for Neutral lipid storage myopathy?

Tomeko shows live, recruiting studies for Neutral lipid storage myopathy 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