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Hereditary painful callosities

Just diagnosed with Hereditary painful callosities?

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

Open the full Hereditary painful callosities hub →

Overview

Hereditary painful callosities is a rare condition. Also known as PPK nummularis, Plamoplantar hyperkeratosis nummularis, Plamoplantar keratoderma nummularis, Keratosis palmoplantaris nummularis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary painful callosities so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:79141 · OMIM 114140 · ICD-10 Q82.8 · GARD 0016705

Find care for Hereditary painful callosities

Authoritative references for Hereditary painful callosities

Common questions

I was just diagnosed with Hereditary painful callosities — what should I do first?

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

Where can I find a specialist for Hereditary painful callosities?

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

Are there clinical trials for Hereditary painful callosities?

Tomeko shows live, recruiting studies for Hereditary painful callosities 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