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Congenital prothrombin deficiency

Just diagnosed with Congenital prothrombin deficiency?

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

Open the full Congenital prothrombin deficiency hub →

Overview

Congenital prothrombin deficiency is a rare condition. Also known as Dysprothrombinemia, Hypoprothrombinemia, Prothrombin deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital prothrombin deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:325 · OMIM 613679 · ICD-10 D68.2 · GARD 0002926

Find care for Congenital prothrombin deficiency

Authoritative references for Congenital prothrombin deficiency

Common questions

I was just diagnosed with Congenital prothrombin deficiency — what should I do first?

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

Where can I find a specialist for Congenital prothrombin deficiency?

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

Are there clinical trials for Congenital prothrombin deficiency?

Tomeko shows live, recruiting studies for Congenital prothrombin 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