Just diagnosed with Familial multiple lipomatosis?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial multiple lipomatosis, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Familial multiple lipomatosis hub →Overview
Familial multiple lipomatosis is a rare condition. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial multiple lipomatosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:199276 · OMIM 151900 · ICD-10 E88.2 · GARD 0012925
Find care for Familial multiple lipomatosis
Authoritative references for Familial multiple lipomatosis
Research & market landscape for Familial multiple lipomatosis
Following Familial multiple lipomatosis for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Familial multiple lipomatosis — the real-world landscape behind the condition, in one place.
- Latest Familial multiple lipomatosis research on PubMed ↗
- Recruiting Familial multiple lipomatosis trials on ClinicalTrials.gov ↗
- Explore the Familial multiple lipomatosis research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Familial multiple lipomatosis and every rare condition. See how Tomeko works with industry →
Common questions
What is Familial multiple lipomatosis?
Familial multiple lipomatosis is a rare condition. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Familial multiple lipomatosis together in one place.
What are the symptoms of Familial multiple lipomatosis?
Symptoms of Familial multiple lipomatosis vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Familial multiple lipomatosis.
How is Familial multiple lipomatosis treated?
Treatment for Familial multiple lipomatosis depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Familial multiple lipomatosis, and review current options with them.
What causes Familial multiple lipomatosis — is it genetic?
The cause and inheritance of Familial multiple lipomatosis are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Familial multiple lipomatosis can explain what it means for you and your family.
I was just diagnosed with Familial multiple lipomatosis — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial multiple lipomatosis, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Familial multiple lipomatosis?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Familial multiple lipomatosis, filtered to your area.
Are there clinical trials for Familial multiple lipomatosis?
Tomeko shows live, recruiting studies for Familial multiple lipomatosis from ClinicalTrials.gov on the hub.
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