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Infantile hypophosphatasia

Just diagnosed with Infantile hypophosphatasia?

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

Open the full Infantile hypophosphatasia hub →

Overview

Infantile hypophosphatasia is a rare condition. Also known as Infantile Rathbun disease, Infantile phosphoethanolaminuria. Tomeko brings together the specialists, research, clinical trials, treatments and community for Infantile hypophosphatasia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:247651 · OMIM 241500 · ICD-10 E83.3 · GARD 0028133

Find care for Infantile hypophosphatasia

Authoritative references for Infantile hypophosphatasia

Common questions

I was just diagnosed with Infantile hypophosphatasia — what should I do first?

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

Where can I find a specialist for Infantile hypophosphatasia?

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

Are there clinical trials for Infantile hypophosphatasia?

Tomeko shows live, recruiting studies for Infantile hypophosphatasia 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