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Congenital factor VII deficiency

Just diagnosed with Congenital factor VII deficiency?

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

Open the full Congenital factor VII deficiency hub →

Overview

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

Identifiers: ORPHA:327 · OMIM 227500 · ICD-10 D68.2 · GARD 0002238

Find care for Congenital factor VII deficiency

Authoritative references for Congenital factor VII deficiency

Common questions

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

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

Where can I find a specialist for Congenital factor VII deficiency?

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

Are there clinical trials for Congenital factor VII deficiency?

Tomeko shows live, recruiting studies for Congenital factor VII 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