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Familial type 5 hyperlipoproteinemia

Just diagnosed with Familial type 5 hyperlipoproteinemia?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial type 5 hyperlipoproteinemia, look for clinical trials, and connect with others living with it — all in one place.

Open the full Familial type 5 hyperlipoproteinemia hub →

Overview

Familial type 5 hyperlipoproteinemia is a rare condition. Also known as Familial APOA5 deficiency, Familial apolipoprotein A-V deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial type 5 hyperlipoproteinemia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:530849 · OMIM 144650, 145750 · ICD-10 E78.3 · GARD 0006704

Find care for Familial type 5 hyperlipoproteinemia

Authoritative references for Familial type 5 hyperlipoproteinemia

Common questions

I was just diagnosed with Familial type 5 hyperlipoproteinemia — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Familial type 5 hyperlipoproteinemia, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Familial type 5 hyperlipoproteinemia?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Familial type 5 hyperlipoproteinemia, filtered to your area.

Are there clinical trials for Familial type 5 hyperlipoproteinemia?

Tomeko shows live, recruiting studies for Familial type 5 hyperlipoproteinemia 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