Just diagnosed with Hypophosphatasia?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hypophosphatasia, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Hypophosphatasia hub →Overview
Hypophosphatasia is a rare condition. Also known as HPP, Phosphoethanolaminuria, Rathbun disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hypophosphatasia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:436 · OMIM 146300, 241500, 241510 · ICD-10 E83.3 · GARD 0006734
Find care for Hypophosphatasia
Patient organizations for Hypophosphatasia
- Avalon Foundation
Authoritative references for Hypophosphatasia
Research & market landscape for Hypophosphatasia
Following Hypophosphatasia for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Hypophosphatasia — the real-world landscape behind the condition, in one place.
- Latest Hypophosphatasia research on PubMed ↗
- Recruiting Hypophosphatasia trials on ClinicalTrials.gov ↗
- Explore the Hypophosphatasia research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Hypophosphatasia and every rare condition. See how Tomeko works with industry →
Common questions
What is Hypophosphatasia?
Hypophosphatasia is a rare condition. Also known as HPP, Phosphoethanolaminuria, Rathbun disease. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Hypophosphatasia together in one place.
What are the symptoms of Hypophosphatasia?
Symptoms of Hypophosphatasia vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Hypophosphatasia.
How is Hypophosphatasia treated?
Treatment for Hypophosphatasia depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Hypophosphatasia, and review current options with them.
What causes Hypophosphatasia — is it genetic?
The cause and inheritance of Hypophosphatasia are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Hypophosphatasia can explain what it means for you and your family.
I was just diagnosed with Hypophosphatasia — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Hypophosphatasia, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Hypophosphatasia?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hypophosphatasia, filtered to your area.
Are there clinical trials for Hypophosphatasia?
Tomeko shows live, recruiting studies for Hypophosphatasia from ClinicalTrials.gov on the hub.
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