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Severe hemophilia B

Just diagnosed with Severe hemophilia B?

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

Open the full Severe hemophilia B hub →

Overview

Severe hemophilia B is a rare condition. Also known as Severe congenital F9 deficiency, Severe congenital factor IX deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Severe hemophilia B so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:169793 · OMIM 306900 · ICD-10 D67 · GARD 0017056

Find care for Severe hemophilia B

Authoritative references for Severe hemophilia B

Common questions

I was just diagnosed with Severe hemophilia B — what should I do first?

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

Where can I find a specialist for Severe hemophilia B?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Severe hemophilia B, filtered to your area.

Are there clinical trials for Severe hemophilia B?

Tomeko shows live, recruiting studies for Severe hemophilia B 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