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Hereditary factor XI deficiency disease

Just diagnosed with Hereditary factor XI deficiency disease?

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

Open the full Hereditary factor XI deficiency disease hub →

Overview

Hereditary factor XI deficiency disease is a rare condition. Also known as Hemophilia C, PTA deficiency, Plasma thromboplastin antecedent deficiency, Rosenthal factor deficiency, Rosenthal syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary factor XI deficiency disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:329 · OMIM 612416 · ICD-10 D68.1 · GARD 0009670

Find care for Hereditary factor XI deficiency disease

Authoritative references for Hereditary factor XI deficiency disease

Common questions

I was just diagnosed with Hereditary factor XI deficiency disease — what should I do first?

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

Where can I find a specialist for Hereditary factor XI deficiency disease?

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

Are there clinical trials for Hereditary factor XI deficiency disease?

Tomeko shows live, recruiting studies for Hereditary factor XI deficiency disease 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