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Hereditary antithrombin deficiency

Just diagnosed with Hereditary antithrombin deficiency?

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

Open the full Hereditary antithrombin deficiency hub →

Overview

Hereditary antithrombin deficiency is a rare condition. Also known as Hereditary thrombophilia due to congenital antithrombin 3 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary antithrombin deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:82 · OMIM 613118 · ICD-10 D68.5 · GARD 0006148

Find care for Hereditary antithrombin deficiency

Authoritative references for Hereditary antithrombin deficiency

Common questions

I was just diagnosed with Hereditary antithrombin deficiency — what should I do first?

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

Where can I find a specialist for Hereditary antithrombin deficiency?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary antithrombin deficiency, filtered to your area.

Are there clinical trials for Hereditary antithrombin deficiency?

Tomeko shows live, recruiting studies for Hereditary antithrombin deficiency 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